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rs56821304

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs56821304(A;A)
Make rs56821304(A;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position52287145
GeneKRT81, KRT86
is asnp
is mentioned by
dbSNPrs56821304
ebirs56821304
HLIrs56821304
Exacrs56821304
Varsomers56821304
Maprs56821304
PheGenIrs56821304
hapmaprs56821304
1000 genomesrs56821304
hgdprs56821304
ensemblrs56821304
gopubmedrs56821304
geneviewrs56821304
scholarrs56821304
googlers56821304
pharmgkbrs56821304
gwascentralrs56821304
openSNPrs56821304
23andMers56821304
23andMe allrs56821304
SNP Nexus

SNPshotrs56821304
SNPdbers56821304
MSV3drs56821304
GWAS Ctlgrs56821304
GMAF0.001837
Max Magnitude0
OMIM602153
Desc
Variant0002
Relatedalso
ClinVar
Risk rs56821304(A,C;A,C)
Alt rs56821304(A,C;A,C)
Reference rs56821304(G;G)
Significance Pathogenic
Disease Beaded hair not provided
Variation info
Gene KRT86 KRT81
CLNDBN Beaded hair not provided
Reversed 1
HGVS NC_000012.11:g.52680929C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007931.2, RCV000056951.1,