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rs61664582

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61664582(G;T)
Make rs61664582(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position41583278
GeneKRT14
is asnp
is mentioned by
dbSNPrs61664582
dbSNP (old)rs61664582
ClinGenrs61664582
ebirs61664582
HLIrs61664582
Exacrs61664582
Gnomadrs61664582
Varsomers61664582
Maprs61664582
PheGenIrs61664582
Biobankrs61664582
1000 genomesrs61664582
hgdprs61664582
ensemblrs61664582
gopubmedrs61664582
geneviewrs61664582
scholarrs61664582
googlers61664582
pharmgkbrs61664582
gwascentralrs61664582
openSNPrs61664582
23andMers61664582
23andMe allrs61664582
SNP Nexus

SNPshotrs61664582
SNPdbers61664582
MSV3drs61664582
GWAS Ctlgrs61664582
Max Magnitude0
ClinVar
Risk rs61664582(A;A) rs61664582(T;T)
Alt rs61664582(A;A) rs61664582(T;T)
Reference Rs61664582(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT14
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.39739530C>A; NC_000017.10:g.39739530C>T
CLNSRC
CLNACC RCV000056678.1, RCV000056677.2,