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rs121908328

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908328(G;T)
Make rs121908328(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position78119382
GeneTMC6
is asnp
is mentioned by
dbSNPrs121908328
ebirs121908328
HLIrs121908328
Exacrs121908328
Varsomers121908328
Maprs121908328
PheGenIrs121908328
hapmaprs121908328
1000 genomesrs121908328
hgdprs121908328
ensemblrs121908328
gopubmedrs121908328
geneviewrs121908328
scholarrs121908328
googlers121908328
pharmgkbrs121908328
gwascentralrs121908328
openSNPrs121908328
23andMers121908328
23andMe allrs121908328
SNP Nexus

SNPshotrs121908328
SNPdbers121908328
MSV3drs121908328
GWAS Ctlgrs121908328
Max Magnitude0
OMIM605828
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908328(A,T;A,T)
Alt rs121908328(A,T;A,T)
Reference rs121908328(G;G)
Significance Pathogenic
Disease EPIDERMODYSPLASIA VERRUCIFORMIS
Variation info
Gene TMC6
CLNDBN EPIDERMODYSPLASIA VERRUCIFORMIS
Reversed 1
HGVS NC_000017.10:g.76115463C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005015.3,