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rs786203009

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203009(A;A)
Make rs786203009(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position65093706
GeneLOC100506321, MAX
is asnp
is mentioned by
dbSNPrs786203009
ebirs786203009
HLIrs786203009
Exacrs786203009
Varsomers786203009
Maprs786203009
PheGenIrs786203009
hapmaprs786203009
1000 genomesrs786203009
hgdprs786203009
ensemblrs786203009
gopubmedrs786203009
geneviewrs786203009
scholarrs786203009
googlers786203009
pharmgkbrs786203009
gwascentralrs786203009
openSNPrs786203009
23andMers786203009
23andMe allrs786203009
SNP Nexus

SNPshotrs786203009
SNPdbers786203009
MSV3drs786203009
GWAS Ctlgrs786203009
Max Magnitude0
ClinVar
Risk rs786203009(A;A)
Alt rs786203009(A;A)
Reference rs786203009(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene LOC100506321 MAX
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000014.8:g.65560424A>T
CLNSRC
CLNACC RCV000166125.1,