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rs796065353

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796065353(A;A)
Make rs796065353(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position219213495
GeneABCB6
is asnp
is mentioned by
dbSNPrs796065353
ebirs796065353
HLIrs796065353
Exacrs796065353
Varsomers796065353
Maprs796065353
PheGenIrs796065353
hapmaprs796065353
1000 genomesrs796065353
hgdprs796065353
ensemblrs796065353
gopubmedrs796065353
geneviewrs796065353
scholarrs796065353
googlers796065353
pharmgkbrs796065353
gwascentralrs796065353
openSNPrs796065353
23andMers796065353
23andMe allrs796065353
SNP Nexus

SNPshotrs796065353
SNPdbers796065353
MSV3drs796065353
GWAS Ctlgrs796065353
Max Magnitude0
ClinVar
Risk rs796065353(A;A)
Alt rs796065353(A;A)
Reference rs796065353(C;C)
Significance Pathogenic
Disease Dyschromatosis universalis hereditaria 3
Variation info
Gene ABCB6
CLNDBN Dyschromatosis universalis hereditaria 3
Reversed 1
HGVS NC_000002.11:g.220078217G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000190414.2,