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rs398122377

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122377(-;-)
Make rs398122377(-;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position53939261
GeneHOXC13, HOXC13-AS
is asnp
is mentioned by
dbSNPrs398122377
ebirs398122377
HLIrs398122377
Exacrs398122377
Varsomers398122377
Maprs398122377
PheGenIrs398122377
hapmaprs398122377
1000 genomesrs398122377
hgdprs398122377
ensemblrs398122377
gopubmedrs398122377
geneviewrs398122377
scholarrs398122377
googlers398122377
pharmgkbrs398122377
gwascentralrs398122377
openSNPrs398122377
23andMers398122377
23andMe allrs398122377
SNP Nexus

SNPshotrs398122377
SNPdbers398122377
MSV3drs398122377
GWAS Ctlgrs398122377
Max Magnitude0
ClinVar
Risk rs398122377(;)
Alt rs398122377(;)
Reference rs398122377(C;C)
Significance Pathogenic
Disease Ectodermal dysplasia 9
Variation info
Gene HOXC13-AS HOXC13
CLNDBN Ectodermal dysplasia 9, hair/nail type
Reversed 0
HGVS NC_000012.11:g.54333045delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000043557.25,