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rs1057520078

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520078(-;-)
Make rs1057520078(-;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position129562637
GeneOCRL
is asnp
is mentioned by
dbSNPrs1057520078
dbSNP (old)rs1057520078
ClinGenrs1057520078
ebirs1057520078
HLIrs1057520078
Exacrs1057520078
Gnomadrs1057520078
Varsomers1057520078
Maprs1057520078
PheGenIrs1057520078
Biobankrs1057520078
1000 genomesrs1057520078
hgdprs1057520078
ensemblrs1057520078
gopubmedrs1057520078
geneviewrs1057520078
scholarrs1057520078
googlers1057520078
pharmgkbrs1057520078
gwascentralrs1057520078
openSNPrs1057520078
23andMers1057520078
23andMe allrs1057520078
SNPshotrs1057520078
SNPdbers1057520078
MSV3drs1057520078
GWAS Ctlgrs1057520078
Max Magnitude0
ClinVar
Risk rs1057520078(-;-)
Alt rs1057520078(-;-)
Reference Rs1057520078(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OCRL
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.128696614delC
CLNSRC
CLNACC RCV000441341.1,