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rs786205480

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205480(G;G)
Make rs786205480(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position52315911
GeneKRT83
is asnp
is mentioned by
dbSNPrs786205480
ebirs786205480
HLIrs786205480
Exacrs786205480
Varsomers786205480
Maprs786205480
PheGenIrs786205480
hapmaprs786205480
1000 genomesrs786205480
hgdprs786205480
ensemblrs786205480
gopubmedrs786205480
geneviewrs786205480
scholarrs786205480
googlers786205480
pharmgkbrs786205480
gwascentralrs786205480
openSNPrs786205480
23andMers786205480
23andMe allrs786205480
SNP Nexus

SNPshotrs786205480
SNPdbers786205480
MSV3drs786205480
GWAS Ctlgrs786205480
Max Magnitude0
ClinVar
Risk rs786205480(G;G)
Alt rs786205480(G;G)
Reference rs786205480(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KRT83
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.52709695A>C
CLNSRC
CLNACC RCV000171215.1,