Have questions? Visit https://www.reddit.com/r/SNPedia

rs60297570

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs60297570(C;T)
Make rs60297570(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position52678650
GeneKRT1
is asnp
is mentioned by
dbSNPrs60297570
dbSNP (classic)rs60297570
ClinGenrs60297570
ebirs60297570
HLIrs60297570
Exacrs60297570
Gnomadrs60297570
Varsomers60297570
LitVarrs60297570
Maprs60297570
PheGenIrs60297570
Biobankrs60297570
1000 genomesrs60297570
hgdprs60297570
ensemblrs60297570
geneviewrs60297570
scholarrs60297570
googlers60297570
pharmgkbrs60297570
gwascentralrs60297570
openSNPrs60297570
23andMers60297570
SNPshotrs60297570
SNPdbers60297570
MSV3drs60297570
GWAS Ctlgrs60297570
Max Magnitude0
ClinVar
Risk rs60297570(T;T)
Alt rs60297570(T;T)
Reference Rs60297570(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT1
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.53072434G>A
CLNSRC
CLNACC RCV000057104.2,