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rs1057518276

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518276(A;G)
Make rs1057518276(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position129562666
GeneOCRL
is asnp
is mentioned by
dbSNPrs1057518276
dbSNP (classic)rs1057518276
ClinGenrs1057518276
ebirs1057518276
HLIrs1057518276
Exacrs1057518276
Gnomadrs1057518276
Varsomers1057518276
LitVarrs1057518276
Maprs1057518276
PheGenIrs1057518276
Biobankrs1057518276
1000 genomesrs1057518276
hgdprs1057518276
ensemblrs1057518276
geneviewrs1057518276
scholarrs1057518276
googlers1057518276
pharmgkbrs1057518276
gwascentralrs1057518276
openSNPrs1057518276
23andMers1057518276
23andMe allrs1057518276
SNPshotrs1057518276
SNPdbers1057518276
MSV3drs1057518276
GWAS Ctlgrs1057518276
Max Magnitude0
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,