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rs786201675

From SNPedia

Orientationplus
Geno Mag Summary
(TTTTA;TTTTA) 0 common in clinvar
Make rs786201675(-;-)
Make rs786201675(-;TTATT)
Make rs786201675(TTATT;TTATT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108282845
GeneATM
is asnp
is mentioned by
dbSNPrs786201675
ebirs786201675
HLIrs786201675
Exacrs786201675
Varsomers786201675
Maprs786201675
PheGenIrs786201675
hapmaprs786201675
1000 genomesrs786201675
hgdprs786201675
ensemblrs786201675
gopubmedrs786201675
geneviewrs786201675
scholarrs786201675
googlers786201675
pharmgkbrs786201675
gwascentralrs786201675
openSNPrs786201675
23andMers786201675
23andMe allrs786201675
SNP Nexus

SNPshotrs786201675
SNPdbers786201675
MSV3drs786201675
GWAS Ctlgrs786201675
Max Magnitude0
ClinVar
Risk rs786201675(;)
Alt rs786201675(;)
Reference rs786201675(TTTTA;TTTTA)
Significance Other
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108153572_108153576delTTATT
CLNSRC
CLNACC RCV000164077.2, RCV000222105.1,