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rs587776845

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776845(-;-)
Make rs587776845(-;TTG)
Make rs587776845(TTG;TTG)
ReferenceGRCh38 38.1/142
Chromosome12
Position52813639
GeneKRT4
is asnp
is mentioned by
dbSNPrs587776845
ebirs587776845
HLIrs587776845
Exacrs587776845
Varsomers587776845
Maprs587776845
PheGenIrs587776845
hapmaprs587776845
1000 genomesrs587776845
hgdprs587776845
ensemblrs587776845
gopubmedrs587776845
geneviewrs587776845
scholarrs587776845
googlers587776845
pharmgkbrs587776845
gwascentralrs587776845
openSNPrs587776845
23andMers587776845
23andMe allrs587776845
SNP Nexus

SNPshotrs587776845
SNPdbers587776845
MSV3drs587776845
GWAS Ctlgrs587776845
Max Magnitude0
ClinVar
Risk rs587776845(TTG;TTG)
Alt rs587776845(TTG;TTG)
Reference rs587776845(;)
Significance Pathogenic
Disease White sponge nevus of cannon
Variation info
Gene KRT4
CLNDBN White sponge nevus of cannon
Reversed 1
HGVS NC_000012.11:g.53207423_53207424insTTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000018421.28,