rs641221

Homo sapiens
A>G
ZFR : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G=0425 (12720/29904,GnomAD)
G=0401 (11683/29118,TOPMED)
G=0443 (2218/5008,1000G)
G=0445 (1715/3854,ALSPAC)
G=0427 (1585/3708,TWINSUK)
chr5:32439218 (GRCh38.p7) (5p13.3)
AD
GWASdb2
2   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 5NC_000005.10:g.32439218A>G
GRCh37.p13 chr 5NC_000005.9:g.32439324A>G

Gene: ZFR, zinc finger RNA binding protein(minus strand)

Molecule type Change Amino acid[Codon] SO Term
ZFR transcriptNM_016107.3:c.N/AIntron Variant
ZFR transcript variant X1XR_427659.2:n.N/AIntron Variant

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr53241085932411060E067-28264
chr53241423532414485E067-24839
chr53241994632420225E067-19099
chr53242072032420906E067-18418
chr53242106832421112E067-18212
chr53242131932421412E067-17912
chr53242156732421624E067-17700
chr53242224032422284E067-17040
chr53242879232428856E067-10468
chr53243934132439502E06717
chr53243959832439715E067274
chr53239094032391592E068-47732
chr53242072032420906E068-18418
chr53242106832421112E068-18212
chr53242131932421412E068-17912
chr53242879232428856E068-10468
chr53243586032435940E068-3384
chr53246144432461596E06822120
chr53246175832461819E06822434
chr53247555632475851E06836232
chr53239094032391592E069-47732
chr53239164932391740E069-47584
chr53242106832421112E069-18212
chr53242131932421412E069-17912
chr53242156732421624E069-17700
chr53242224032422284E069-17040
chr53242413232424233E069-15091
chr53243934132439502E06917
chr53239094032391592E071-47732
chr53241423532414485E071-24839
chr53241994632420225E071-19099
chr53242072032420906E071-18418
chr53242106832421112E071-18212
chr53242131932421412E071-17912
chr53242156732421624E071-17700
chr53242224032422284E071-17040
chr53242413232424233E071-15091
chr53242427932424341E071-14983
chr53243683532436958E071-2366
chr53243700532437193E071-2131
chr53243934132439502E07117
chr53243959832439715E071274
chr53244558532445902E0716261
chr53239094032391592E072-47732
chr53239164932391740E072-47584
chr53241085932411060E072-28264
chr53241994632420225E072-19099
chr53242072032420906E072-18418
chr53243538232435557E072-3767
chr53243959832439715E072274
chr53243981332439873E072489
chr53244558532445902E0726261
chr53241994632420225E073-19099
chr53242072032420906E073-18418
chr53243586032435940E073-3384
chr53244558532445902E0736261
chr53239083632390905E074-48419
chr53239094032391592E074-47732
chr53239164932391740E074-47584
chr53239224032392412E074-46912
chr53241085932411060E074-28264
chr53241210732412211E074-27113
chr53241273132412871E074-26453
chr53241423532414485E074-24839
chr53242413232424233E074-15091
chr53242427932424341E074-14983
chr53242879232428856E074-10468
chr53243934132439502E07417
chr53243959832439715E074274
chr53244558532445902E0746261
chr53244558532445902E0816261
chr53244600532446066E0816681








Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr53244321832445582E0673894
chr53244321832445582E0683894
chr53244321832445582E0693894
chr53244321832445582E0703894
chr53244321832445582E0713894
chr53244321832445582E0723894
chr53244321832445582E0733894
chr53244321832445582E0743894
chr53244321832445582E0813894
chr53244321832445582E0823894










Mpgyi