SNP Detail Info-rs10158567

Sequence Name	Change(s)
GRCh38.p7 chr 1	NC_000001.11:g.241125210G>A
GRCh37.p13 chr 1	NC_000001.10:g.241288510G>A

Molecule type	Change	Amino acid[Codon]	SO Term
RGS7 transcript variant 2	NM_001282773.1:c.	N/A	Intron Variant
RGS7 transcript variant 3	NM_001282775.1:c.	N/A	Intron Variant
RGS7 transcript variant 4	NM_001282778.1:c.	N/A	Intron Variant
RGS7 transcript variant 1	NM_002924.5:c.	N/A	Intron Variant
RGS7 transcript variant X1	XM_005273218.3:c.	N/A	Intron Variant
RGS7 transcript variant X5	XM_011544246.2:c.	N/A	Intron Variant
RGS7 transcript variant X2	XM_017002001.1:c.	N/A	Intron Variant
RGS7 transcript variant X3	XM_017002002.1:c.	N/A	Intron Variant
RGS7 transcript variant X7	XM_017002003.1:c.	N/A	Intron Variant
RGS7 transcript variant X8	XM_017002004.1:c.	N/A	Intron Variant
RGS7 transcript variant X9	XM_017002005.1:c.	N/A	Intron Variant
RGS7 transcript variant X10	XM_017002006.1:c.	N/A	Intron Variant
RGS7 transcript variant X11	XM_017002007.1:c.	N/A	Intron Variant
RGS7 transcript variant X12	XM_017002008.1:c.	N/A	Intron Variant
RGS7 transcript variant X14	XM_017002010.1:c.	N/A	Intron Variant
RGS7 transcript variant X4	XM_006711800.3:c.	N/A	Genic Upstream Transcript Variant
RGS7 transcript variant X6	XM_011544247.2:c.	N/A	Genic Upstream Transcript Variant
RGS7 transcript variant X10	XM_017002009.1:c.	N/A	Genic Upstream Transcript Variant
RGS7 transcript variant X15	XM_017002011.1:c.	N/A	Genic Upstream Transcript Variant
RGS7 transcript variant X16	XM_017002012.1:c.	N/A	Genic Upstream Transcript Variant
RGS7 transcript variant X13	XM_017002013.1:c.	N/A	Genic Upstream Transcript Variant

Study	Population	Group	Sample #	Ref Allele	Alt Allele
1000Genomes	African	Sub	1322	G=0.143	A=0.857
1000Genomes	American	Sub	694	G=0.680	A=0.320
1000Genomes	East Asian	Sub	1008	G=0.622	A=0.378
1000Genomes	Europe	Sub	1006	G=0.745	A=0.255
1000Genomes	Global	Study-wide	5008	G=0.552	A=0.448
1000Genomes	South Asian	Sub	978	G=0.740	A=0.260
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.740	A=0.260
The Genome Aggregation Database	African	Sub	8698	G=0.217	A=0.783
The Genome Aggregation Database	American	Sub	836	G=0.730	A=0.270
The Genome Aggregation Database	East Asian	Sub	1610	G=0.586	A=0.414
The Genome Aggregation Database	Europe	Sub	18438	G=0.769	A=0.230
The Genome Aggregation Database	Global	Study-wide	29882	G=0.597	A=0.402
The Genome Aggregation Database	Other	Sub	300	G=0.750	A=0.250
Trans-Omics for Precision Medicine	Global	Study-wide	29116	G=0.509	A=0.491
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.742	A=0.258

Chromosome	Start	End	Region	Distance ( -/+ : Up/Downstream )
chr1	241242355	241242698	E073	-45812
chr1	241307188	241307332	E081	18678
chr1	241321839	241321911	E082	33329

rs10158567