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rs786202318

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(GAATGGTGCACAG;GAATGGTGCACAG) 0 common in clinvar
Make rs786202318(-;-)
Make rs786202318(-;TGGTGCACAGGAA)
Make rs786202318(TGGTGCACAGGAA;TGGTGCACAGGAA)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108343258
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786202318
dbSNP (old)rs786202318
ClinGenrs786202318
ebirs786202318
HLIrs786202318
Exacrs786202318
Gnomadrs786202318
Varsomers786202318
Maprs786202318
PheGenIrs786202318
Biobankrs786202318
1000 genomesrs786202318
hgdprs786202318
ensemblrs786202318
gopubmedrs786202318
geneviewrs786202318
scholarrs786202318
googlers786202318
pharmgkbrs786202318
gwascentralrs786202318
openSNPrs786202318
23andMers786202318
23andMe allrs786202318
SNP Nexus

SNPshotrs786202318
SNPdbers786202318
MSV3drs786202318
GWAS Ctlgrs786202318
Max Magnitude0
ClinVar
Risk rs786202318(-;-)
Alt rs786202318(-;-)
Reference Rs786202318(GAATGGTGCACAG;GAATGGTGCACAG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108213985_108213997delTGGTGCACAGGAA
CLNSRC
CLNACC RCV000165065.1, RCV000484455.1,