rs1057519627

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1057519627(G;T)

Make rs1057519627(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

Y

Position

2787377

Gene

SRY

is a	snp
is	mentioned by
dbSNP	rs1057519627
dbSNP (classic)	rs1057519627
ClinGen	rs1057519627
ebi	rs1057519627
HLI	rs1057519627
Exac	rs1057519627
Gnomad	rs1057519627
Varsome	rs1057519627
LitVar	rs1057519627
Map	rs1057519627
PheGenI	rs1057519627
Biobank	rs1057519627
1000 genomes	rs1057519627
hgdp	rs1057519627
ensembl	rs1057519627
geneview	rs1057519627
scholar	rs1057519627
google	rs1057519627
pharmgkb	rs1057519627
gwascentral	rs1057519627
openSNP	rs1057519627
23andMe	rs1057519627
SNPshot	rs1057519627
SNPdbe	rs1057519627
MSV3d	rs1057519627
GWAS Ctlg	rs1057519627

Y Chrom

rs1057519627

Max Magnitude

0

ClinVar
Risk	rs1057519627(T;T)
Alt	rs1057519627(T;T)
Reference	Rs1057519627(G;G)
Significance	Probable-Pathogenic
Disease	46
Variation	info
Gene	SRY
CLNDBN	46,XY sex reversal, type 1
Reversed	1
HGVS	NC_000024.9:g.2655418C>A
CLNSRC
CLNACC	RCV000445559.1,