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rs587776844

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAAG;CAAG) 0 common in clinvar
(TTG;TTG) 0 common in clinvar
Make rs587776844(-;-)
Make rs587776844(-;TTG)
ReferenceGRCh38 38.1/142
Chromosome12
Position52813619
GeneKRT4
is asnp
is mentioned by
dbSNPrs587776844
ebirs587776844
HLIrs587776844
Exacrs587776844
Varsomers587776844
Maprs587776844
PheGenIrs587776844
hapmaprs587776844
1000 genomesrs587776844
hgdprs587776844
ensemblrs587776844
gopubmedrs587776844
geneviewrs587776844
scholarrs587776844
googlers587776844
pharmgkbrs587776844
gwascentralrs587776844
openSNPrs587776844
23andMers587776844
23andMe allrs587776844
SNP Nexus

SNPshotrs587776844
SNPdbers587776844
MSV3drs587776844
GWAS Ctlgrs587776844
Max Magnitude0
ClinVar
Risk rs587776844(TTGG,G;TTGG,G)
Alt rs587776844(TTGG,G;TTGG,G)
Reference rs587776844(CAAG;CAAG)
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.53207403_53207405delTTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000018420.28,