rs1057518276

Orientation

plus

Stabilized

plus

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

Make rs1057518276(A;G)

Make rs1057518276(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

129562666

Gene

OCRL

is a	snp
is	mentioned by
dbSNP	rs1057518276
dbSNP (classic)	rs1057518276
ClinGen	rs1057518276
ebi	rs1057518276
HLI	rs1057518276
Exac	rs1057518276
Gnomad	rs1057518276
Varsome	rs1057518276
LitVar	rs1057518276
Map	rs1057518276
PheGenI	rs1057518276
Biobank	rs1057518276
1000 genomes	rs1057518276
hgdp	rs1057518276
ensembl	rs1057518276
geneview	rs1057518276
scholar	rs1057518276
google	rs1057518276
pharmgkb	rs1057518276
gwascentral	rs1057518276
openSNP	rs1057518276
23andMe	rs1057518276
SNPshot	rs1057518276
SNPdbe	rs1057518276
MSV3d	rs1057518276
GWAS Ctlg	rs1057518276

Max Magnitude

0

ClinVar
Risk	rs1057518276(G;G)
Alt	rs1057518276(G;G)
Reference	Rs1057518276(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	OCRL
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.128696643A>G
CLNSRC
CLNACC	RCV000412922.1,