rs1057521742

Orientation

plus

Stabilized

plus

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

Make rs1057521742(A;A)

Make rs1057521742(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

129562484

Gene

OCRL

is a	snp
is	mentioned by
dbSNP	rs1057521742
dbSNP (classic)	rs1057521742
ClinGen	rs1057521742
ebi	rs1057521742
HLI	rs1057521742
Exac	rs1057521742
Gnomad	rs1057521742
Varsome	rs1057521742
LitVar	rs1057521742
Map	rs1057521742
PheGenI	rs1057521742
Biobank	rs1057521742
1000 genomes	rs1057521742
hgdp	rs1057521742
ensembl	rs1057521742
geneview	rs1057521742
scholar	rs1057521742
google	rs1057521742
pharmgkb	rs1057521742
gwascentral	rs1057521742
openSNP	rs1057521742
23andMe	rs1057521742
SNPshot	rs1057521742
SNPdbe	rs1057521742
MSV3d	rs1057521742
GWAS Ctlg	rs1057521742

Max Magnitude

0

ClinVar
Risk	rs1057521742(A;A)
Alt	rs1057521742(A;A)
Reference	Rs1057521742(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	OCRL
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.128696461G>A
CLNSRC
CLNACC	RCV000424806.1,