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rs587776602

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776602(C;T)
Make rs587776602(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position142741802
GeneSLURP1
is asnp
is mentioned by
dbSNPrs587776602
ebirs587776602
HLIrs587776602
Exacrs587776602
Varsomers587776602
Maprs587776602
PheGenIrs587776602
hapmaprs587776602
1000 genomesrs587776602
hgdprs587776602
ensemblrs587776602
gopubmedrs587776602
geneviewrs587776602
scholarrs587776602
googlers587776602
pharmgkbrs587776602
gwascentralrs587776602
openSNPrs587776602
23andMers587776602
23andMe allrs587776602
SNP Nexus

SNPshotrs587776602
SNPdbers587776602
MSV3drs587776602
GWAS Ctlgrs587776602
Max Magnitude0
ClinVar
Risk rs587776602(C,T;C,T)
Alt rs587776602(C,T;C,T)
Reference rs587776602(G;G)
Significance Pathogenic
Disease Acroerythrokeratoderma
Variation info
Gene SLURP1
CLNDBN Acroerythrokeratoderma
Reversed 1
HGVS NC_000008.10:g.143823220C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004863.3,