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rs60090257

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs60090257(A;A)
Make rs60090257(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome17
Position41583772
GeneKRT14
is asnp
is mentioned by
dbSNPrs60090257
dbSNP (classic)rs60090257
ClinGenrs60090257
ebirs60090257
HLIrs60090257
Exacrs60090257
Gnomadrs60090257
Varsomers60090257
LitVarrs60090257
Maprs60090257
PheGenIrs60090257
Biobankrs60090257
1000 genomesrs60090257
hgdprs60090257
ensemblrs60090257
geneviewrs60090257
scholarrs60090257
googlers60090257
pharmgkbrs60090257
gwascentralrs60090257
openSNPrs60090257
23andMers60090257
23andMe allrs60090257
SNPshotrs60090257
SNPdbers60090257
MSV3drs60090257
GWAS Ctlgrs60090257
Max Magnitude0
ClinVar
Risk rs60090257(A;A)
Alt rs60090257(A;A)
Reference Rs60090257(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT14
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.39740024C>T
CLNSRC
CLNACC RCV000056757.2,