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rs1057521742

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521742(A;A)
Make rs1057521742(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position129562484
GeneOCRL
is asnp
is mentioned by
dbSNPrs1057521742
dbSNP (old)rs1057521742
ClinGenrs1057521742
ebirs1057521742
HLIrs1057521742
Exacrs1057521742
Gnomadrs1057521742
Varsomers1057521742
Maprs1057521742
PheGenIrs1057521742
Biobankrs1057521742
1000 genomesrs1057521742
hgdprs1057521742
ensemblrs1057521742
gopubmedrs1057521742
geneviewrs1057521742
scholarrs1057521742
googlers1057521742
pharmgkbrs1057521742
gwascentralrs1057521742
openSNPrs1057521742
23andMers1057521742
23andMe allrs1057521742
SNPshotrs1057521742
SNPdbers1057521742
MSV3drs1057521742
GWAS Ctlgrs1057521742
Max Magnitude0
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,