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rs59685571

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs59685571(A;A)
Make rs59685571(A;C)
ReferenceGRCh38 38.1/142
Chromosome12
Position52492676
GeneKRT6A
is asnp
is mentioned by
dbSNPrs59685571
ebirs59685571
HLIrs59685571
Exacrs59685571
Varsomers59685571
Maprs59685571
PheGenIrs59685571
hapmaprs59685571
1000 genomesrs59685571
hgdprs59685571
ensemblrs59685571
gopubmedrs59685571
geneviewrs59685571
scholarrs59685571
googlers59685571
pharmgkbrs59685571
gwascentralrs59685571
openSNPrs59685571
23andMers59685571
23andMe allrs59685571
SNP Nexus

SNPshotrs59685571
SNPdbers59685571
MSV3drs59685571
GWAS Ctlgrs59685571
Max Magnitude0


ClinVar
Risk rs59685571(A;A)
Alt rs59685571(A;A)
Reference rs59685571(C;C)
Significance Pathogenic
Disease not provided PC-K6a
Variation info
Gene KRT6A
CLNDBN not provided PC-K6a
Reversed 1
HGVS NC_000012.11:g.52886460G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000057011.1, RCV000128821.4,