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rs61027685

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61027685(G;T)
Make rs61027685(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position41586438
GeneKRT14
is asnp
is mentioned by
dbSNPrs61027685
dbSNP (old)rs61027685
ClinGenrs61027685
ebirs61027685
HLIrs61027685
Exacrs61027685
Gnomadrs61027685
Varsomers61027685
Maprs61027685
PheGenIrs61027685
Biobankrs61027685
1000 genomesrs61027685
hgdprs61027685
ensemblrs61027685
gopubmedrs61027685
geneviewrs61027685
scholarrs61027685
googlers61027685
pharmgkbrs61027685
gwascentralrs61027685
openSNPrs61027685
23andMers61027685
23andMe allrs61027685
SNP Nexus

SNPshotrs61027685
SNPdbers61027685
MSV3drs61027685
GWAS Ctlgrs61027685
Max Magnitude0
ClinVar
Risk rs61027685(A;A) rs61027685(C;C) rs61027685(T;T)
Alt rs61027685(A;A) rs61027685(C;C) rs61027685(T;T)
Reference Rs61027685(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT14
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.39742690C>A; NC_000017.10:g.39742690C>G; NC_000017.10:g.39742690C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000056729.1, RCV000056728.1, RCV000056727.2,