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rs58556099

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs58556099(A;G)
Make rs58556099(G;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position52492677
GeneKRT6A
is asnp
is mentioned by
dbSNPrs58556099
ebirs58556099
HLIrs58556099
Exacrs58556099
Varsomers58556099
Maprs58556099
PheGenIrs58556099
hapmaprs58556099
1000 genomesrs58556099
hgdprs58556099
ensemblrs58556099
gopubmedrs58556099
geneviewrs58556099
scholarrs58556099
googlers58556099
pharmgkbrs58556099
gwascentralrs58556099
openSNPrs58556099
23andMers58556099
23andMe allrs58556099
SNP Nexus

SNPshotrs58556099
SNPdbers58556099
MSV3drs58556099
GWAS Ctlgrs58556099
Max Magnitude0


ClinVar
Risk rs58556099(C,G;C,G)
Alt rs58556099(C,G;C,G)
Reference rs58556099(A;A)
Significance Pathogenic
Disease not provided PC-K6a
Variation info
Gene KRT6A
CLNDBN not provided PC-K6a
Reversed 1
HGVS NC_000012.11:g.52886461T>C; NC_000012.11:g.52886461T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000057010.1, RCV000128820.4, RCV000057009.1,