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rs1057520613

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520613(A;C)
Make rs1057520613(C;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position129569370
GeneOCRL
is asnp
is mentioned by
dbSNPrs1057520613
dbSNP (old)rs1057520613
ClinGenrs1057520613
ebirs1057520613
HLIrs1057520613
Exacrs1057520613
Gnomadrs1057520613
Varsomers1057520613
LitVarrs1057520613
Maprs1057520613
PheGenIrs1057520613
Biobankrs1057520613
1000 genomesrs1057520613
hgdprs1057520613
ensemblrs1057520613
gopubmedrs1057520613
geneviewrs1057520613
scholarrs1057520613
googlers1057520613
pharmgkbrs1057520613
gwascentralrs1057520613
openSNPrs1057520613
23andMers1057520613
23andMe allrs1057520613
SNPshotrs1057520613
SNPdbers1057520613
MSV3drs1057520613
GWAS Ctlgrs1057520613
Max Magnitude0
ClinVar
Risk rs1057520613(C;C)
Alt rs1057520613(C;C)
Reference Rs1057520613(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OCRL
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.128703347A>C
CLNSRC
CLNACC RCV000430869.1,