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rs60687604

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in complete genomics
Make rs60687604(A;A)
Make rs60687604(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position52306237
GeneKRT86
is asnp
is mentioned by
dbSNPrs60687604
ebirs60687604
HLIrs60687604
Exacrs60687604
Varsomers60687604
Maprs60687604
PheGenIrs60687604
hapmaprs60687604
1000 genomesrs60687604
hgdprs60687604
ensemblrs60687604
gopubmedrs60687604
geneviewrs60687604
scholarrs60687604
googlers60687604
pharmgkbrs60687604
gwascentralrs60687604
openSNPrs60687604
23andMers60687604
23andMe allrs60687604
SNP Nexus

SNPshotrs60687604
SNPdbers60687604
MSV3drs60687604
GWAS Ctlgrs60687604
Merged fromRs28939669
Max Magnitude0
OMIM601928
Desc
Variant0003
Relatedalso
OMIM601928
Desc
Variant0005
Relatedalso
ClinVar
Risk rs60687604(A,C;A,C)
Alt rs60687604(A,C;A,C)
Reference rs60687604(G;G)
Significance Pathogenic
Disease Beaded hair not provided
Variation info
Gene KRT86
CLNDBN Beaded hair not provided
Reversed 0
HGVS NC_000012.11:g.52700021G>A; NC_000012.11:g.52700021G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008050.3, RCV000056957.1, RCV000008052.3, RCV000056958.1,