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rs60612575

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0
Make rs60612575(A;A)
Make rs60612575(A;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position52302269
GeneKRT86
is asnp
is mentioned by
dbSNPrs60612575
ebirs60612575
HLIrs60612575
Exacrs60612575
Varsomers60612575
Maprs60612575
PheGenIrs60612575
hapmaprs60612575
1000 genomesrs60612575
hgdprs60612575
ensemblrs60612575
gopubmedrs60612575
geneviewrs60612575
scholarrs60612575
googlers60612575
pharmgkbrs60612575
gwascentralrs60612575
openSNPrs60612575
23andMers60612575
23andMe allrs60612575
SNP Nexus

SNPshotrs60612575
SNPdbers60612575
MSV3drs60612575
GWAS Ctlgrs60612575
Max Magnitude0
OMIM601928
Desc
Variant0006
Relatedalso
ClinVar
Risk rs60612575(A;A)
Alt rs60612575(A;A)
Reference rs60612575(C;C)
Significance Pathogenic
Disease Beaded hair not provided
Variation info
Gene KRT86
CLNDBN Beaded hair not provided
Reversed 0
HGVS NC_000012.11:g.52696053C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008053.3, RCV000056965.1,