rs1057521952

Orientation

plus

Stabilized

plus

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

Make rs1057521952(C;T)

Make rs1057521952(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

129569367

Gene

OCRL

is a	snp
is	mentioned by
dbSNP	rs1057521952
dbSNP (classic)	rs1057521952
ClinGen	rs1057521952
ebi	rs1057521952
HLI	rs1057521952
Exac	rs1057521952
Gnomad	rs1057521952
Varsome	rs1057521952
LitVar	rs1057521952
Map	rs1057521952
PheGenI	rs1057521952
Biobank	rs1057521952
1000 genomes	rs1057521952
hgdp	rs1057521952
ensembl	rs1057521952
geneview	rs1057521952
scholar	rs1057521952
google	rs1057521952
pharmgkb	rs1057521952
gwascentral	rs1057521952
openSNP	rs1057521952
23andMe	rs1057521952
SNPshot	rs1057521952
SNPdbe	rs1057521952
MSV3d	rs1057521952
GWAS Ctlg	rs1057521952

Max Magnitude

0

ClinVar
Risk	rs1057521952(T;T)
Alt	rs1057521952(T;T)
Reference	Rs1057521952(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	OCRL
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.128703344C>T
CLNSRC
CLNACC	RCV000434372.1,