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rs786203631

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203631(C;C)
Make rs786203631(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108365219
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786203631
ebirs786203631
HLIrs786203631
Exacrs786203631
Varsomers786203631
Maprs786203631
PheGenIrs786203631
hapmaprs786203631
1000 genomesrs786203631
hgdprs786203631
ensemblrs786203631
gopubmedrs786203631
geneviewrs786203631
scholarrs786203631
googlers786203631
pharmgkbrs786203631
gwascentralrs786203631
openSNPrs786203631
23andMers786203631
23andMe allrs786203631
SNP Nexus

SNPshotrs786203631
SNPdbers786203631
MSV3drs786203631
GWAS Ctlgrs786203631
Max Magnitude0
ClinVar
Risk rs786203631(C;C)
Alt rs786203631(C;C)
Reference rs786203631(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108235946G>C
CLNSRC
CLNACC RCV000167026.1,