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rs59897026

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs59897026(C;C)
Make rs59897026(C;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position41505219
GeneKRT13
is asnp
is mentioned by
dbSNPrs59897026
ebirs59897026
HLIrs59897026
Exacrs59897026
Varsomers59897026
Maprs59897026
PheGenIrs59897026
hapmaprs59897026
1000 genomesrs59897026
hgdprs59897026
ensemblrs59897026
gopubmedrs59897026
geneviewrs59897026
scholarrs59897026
googlers59897026
pharmgkbrs59897026
gwascentralrs59897026
openSNPrs59897026
23andMers59897026
23andMe allrs59897026
SNP Nexus

SNPshotrs59897026
SNPdbers59897026
MSV3drs59897026
GWAS Ctlgrs59897026
Max Magnitude0


ClinVar
Risk rs59897026(C;C)
Alt rs59897026(C;C)
Reference rs59897026(T;T)
Significance Pathogenic
Disease not provided White sponge nevus 2
Variation info
Gene KRT13
CLNDBN not provided White sponge nevus 2
Reversed 1
HGVS NC_000017.10:g.39661471A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000057206.1, RCV000116204.2,