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rs1057517951

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517951(C;C)
Make rs1057517951(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position48517259
GenePORCN
is asnp
is mentioned by
dbSNPrs1057517951
dbSNP (classic)rs1057517951
ClinGenrs1057517951
ebirs1057517951
HLIrs1057517951
Exacrs1057517951
Gnomadrs1057517951
Varsomers1057517951
LitVarrs1057517951
Maprs1057517951
PheGenIrs1057517951
Biobankrs1057517951
1000 genomesrs1057517951
hgdprs1057517951
ensemblrs1057517951
geneviewrs1057517951
scholarrs1057517951
googlers1057517951
pharmgkbrs1057517951
gwascentralrs1057517951
openSNPrs1057517951
23andMers1057517951
23andMe allrs1057517951
SNPshotrs1057517951
SNPdbers1057517951
MSV3drs1057517951
GWAS Ctlgrs1057517951
Max Magnitude0
ClinVar
Risk rs1057517951(C;C)
Alt rs1057517951(C;C)
Reference Rs1057517951(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PORCN
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.48375647T>C
CLNSRC
CLNACC RCV000414381.1,