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rs1057521952

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521952(C;T)
Make rs1057521952(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position129569367
GeneOCRL
is asnp
is mentioned by
dbSNPrs1057521952
dbSNP (old)rs1057521952
ClinGenrs1057521952
ebirs1057521952
HLIrs1057521952
Exacrs1057521952
Gnomadrs1057521952
Varsomers1057521952
Maprs1057521952
PheGenIrs1057521952
Biobankrs1057521952
1000 genomesrs1057521952
hgdprs1057521952
ensemblrs1057521952
gopubmedrs1057521952
geneviewrs1057521952
scholarrs1057521952
googlers1057521952
pharmgkbrs1057521952
gwascentralrs1057521952
openSNPrs1057521952
23andMers1057521952
23andMe allrs1057521952
SNPshotrs1057521952
SNPdbers1057521952
MSV3drs1057521952
GWAS Ctlgrs1057521952
Max Magnitude0
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,