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rs587781245

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781245(A;A)
Make rs587781245(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position148533885
GeneSASH1
is asnp
is mentioned by
dbSNPrs587781245
ebirs587781245
HLIrs587781245
Exacrs587781245
Varsomers587781245
Maprs587781245
PheGenIrs587781245
hapmaprs587781245
1000 genomesrs587781245
hgdprs587781245
ensemblrs587781245
gopubmedrs587781245
geneviewrs587781245
scholarrs587781245
googlers587781245
pharmgkbrs587781245
gwascentralrs587781245
openSNPrs587781245
23andMers587781245
23andMe allrs587781245
SNP Nexus

SNPshotrs587781245
SNPdbers587781245
MSV3drs587781245
GWAS Ctlgrs587781245
Max Magnitude0
ClinVar
Risk rs587781245(A;A)
Alt rs587781245(A;A)
Reference rs587781245(G;G)
Significance Probable-Pathogenic
Disease Alopecia Palmoplantar keratoderma dyschromatosis spino-cellular carcinoma ungueal dystrophy
Variation info
Gene SASH1
CLNDBN Alopecia Palmoplantar keratoderma dyschromatosis spino-cellular carcinoma ungueal dystrophy
Reversed 0
HGVS NC_000006.11:g.148855021G>A
CLNSRC
CLNACC RCV000144361.1,