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rs587776689

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776689(A;A)
Make rs587776689(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position95453587
GenePTCH1
is asnp
is mentioned by
dbSNPrs587776689
ebirs587776689
HLIrs587776689
Exacrs587776689
Varsomers587776689
Maprs587776689
PheGenIrs587776689
hapmaprs587776689
1000 genomesrs587776689
hgdprs587776689
ensemblrs587776689
gopubmedrs587776689
geneviewrs587776689
scholarrs587776689
googlers587776689
pharmgkbrs587776689
gwascentralrs587776689
openSNPrs587776689
23andMers587776689
23andMe allrs587776689
SNP Nexus

SNPshotrs587776689
SNPdbers587776689
MSV3drs587776689
GWAS Ctlgrs587776689
Max Magnitude0
ClinVar
Risk rs587776689(A;A)
Alt rs587776689(A;A)
Reference rs587776689(T;T)
Significance Pathogenic
Disease Basal cell carcinoma
Variation info
Gene PTCH1
CLNDBN Basal cell carcinoma, somatic
Reversed 0
HGVS NC_000009.11:g.98215869T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008703.4,