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rs398124617

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124617(-;-)
Make rs398124617(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position48511408
GenePORCN
is asnp
is mentioned by
dbSNPrs398124617
ebirs398124617
HLIrs398124617
Exacrs398124617
Varsomers398124617
Maprs398124617
PheGenIrs398124617
hapmaprs398124617
1000 genomesrs398124617
hgdprs398124617
ensemblrs398124617
gopubmedrs398124617
geneviewrs398124617
scholarrs398124617
googlers398124617
pharmgkbrs398124617
gwascentralrs398124617
openSNPrs398124617
23andMers398124617
23andMe allrs398124617
SNP Nexus

SNPshotrs398124617
SNPdbers398124617
MSV3drs398124617
GWAS Ctlgrs398124617
Max Magnitude0
ClinVar
Risk rs398124617(;)
Alt rs398124617(;)
Reference rs398124617(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PORCN
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.48369796delC
CLNSRC ClinVar
CLNACC RCV000082827.4,