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rs60440396

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs60440396(C;C)
Make rs60440396(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position41505195
GeneKRT13
is asnp
is mentioned by
dbSNPrs60440396
ebirs60440396
HLIrs60440396
Exacrs60440396
Varsomers60440396
Maprs60440396
PheGenIrs60440396
hapmaprs60440396
1000 genomesrs60440396
hgdprs60440396
ensemblrs60440396
gopubmedrs60440396
geneviewrs60440396
scholarrs60440396
googlers60440396
pharmgkbrs60440396
gwascentralrs60440396
openSNPrs60440396
23andMers60440396
23andMe allrs60440396
SNP Nexus

SNPshotrs60440396
SNPdbers60440396
MSV3drs60440396
GWAS Ctlgrs60440396
Max Magnitude0
OMIM148065
Desc
Variant0001
Relatedalso


ClinVar
Risk rs60440396(C;C)
Alt rs60440396(C;C)
Reference rs60440396(T;T)
Significance Pathogenic
Disease White sponge nevus 2 not provided
Variation info
Gene KRT13
CLNDBN White sponge nevus 2 not provided
Reversed 1
HGVS NC_000017.10:g.39661447A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000015734.22, RCV000057210.1,