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rs1057524593

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524593(A;C)
Make rs1057524593(C;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position48514238
GenePORCN
is asnp
is mentioned by
dbSNPrs1057524593
dbSNP (old)rs1057524593
ClinGenrs1057524593
ebirs1057524593
HLIrs1057524593
Exacrs1057524593
Gnomadrs1057524593
Varsomers1057524593
LitVarrs1057524593
Maprs1057524593
PheGenIrs1057524593
Biobankrs1057524593
1000 genomesrs1057524593
hgdprs1057524593
ensemblrs1057524593
gopubmedrs1057524593
geneviewrs1057524593
scholarrs1057524593
googlers1057524593
pharmgkbrs1057524593
gwascentralrs1057524593
openSNPrs1057524593
23andMers1057524593
23andMe allrs1057524593
SNPshotrs1057524593
SNPdbers1057524593
MSV3drs1057524593
GWAS Ctlgrs1057524593
Max Magnitude0
ClinVar
Risk rs1057524593(C;C)
Alt rs1057524593(C;C)
Reference Rs1057524593(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PORCN
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.48372626A>C
CLNSRC
CLNACC RCV000438464.1,