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rs111448623

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111448623(C;C)
Make rs111448623(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position52515795
GeneKRT5
is asnp
is mentioned by
dbSNPrs111448623
dbSNP (old)rs111448623
ClinGenrs111448623
ebirs111448623
HLIrs111448623
Exacrs111448623
Gnomadrs111448623
Varsomers111448623
Maprs111448623
PheGenIrs111448623
Biobankrs111448623
1000 genomesrs111448623
hgdprs111448623
ensemblrs111448623
gopubmedrs111448623
geneviewrs111448623
scholarrs111448623
googlers111448623
pharmgkbrs111448623
gwascentralrs111448623
openSNPrs111448623
23andMers111448623
23andMe allrs111448623
SNPshotrs111448623
SNPdbers111448623
MSV3drs111448623
GWAS Ctlgrs111448623
Max Magnitude0
ClinVar
Risk rs111448623(C;C) rs111448623(G;G)
Alt rs111448623(C;C) rs111448623(G;G)
Reference Rs111448623(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KRT5
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52909579T>G
CLNSRC
CLNACC RCV000445055.1,