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rs57802288

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs57802288(A;A)
Make rs57802288(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position52315936
GeneKRT83
is asnp
is mentioned by
dbSNPrs57802288
ebirs57802288
HLIrs57802288
Exacrs57802288
Varsomers57802288
Maprs57802288
PheGenIrs57802288
hapmaprs57802288
1000 genomesrs57802288
hgdprs57802288
ensemblrs57802288
gopubmedrs57802288
geneviewrs57802288
scholarrs57802288
googlers57802288
pharmgkbrs57802288
gwascentralrs57802288
openSNPrs57802288
23andMers57802288
23andMe allrs57802288
SNP Nexus

SNPshotrs57802288
SNPdbers57802288
MSV3drs57802288
GWAS Ctlgrs57802288
Max Magnitude0
OMIM602765
Desc
Variant0001
Relatedalso
ClinVar
Risk rs57802288(A;A)
Alt rs57802288(A;A)
Reference rs57802288(G;G)
Significance Pathogenic
Disease Beaded hair not provided
Variation info
Gene KRT83
CLNDBN Beaded hair not provided
Reversed 1
HGVS NC_000012.11:g.52709720C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007239.3, RCV000056954.1,