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rs786204726

From SNPedia

Orientationplus
Geno Mag Summary
(TGAC;TGAC) 0 common in clinvar
Make rs786204726(-;-)
Make rs786204726(-;ACTG)
Make rs786204726(ACTG;ACTG)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108365107
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786204726
ebirs786204726
HLIrs786204726
Exacrs786204726
Varsomers786204726
Maprs786204726
PheGenIrs786204726
hapmaprs786204726
1000 genomesrs786204726
hgdprs786204726
ensemblrs786204726
gopubmedrs786204726
geneviewrs786204726
scholarrs786204726
googlers786204726
pharmgkbrs786204726
gwascentralrs786204726
openSNPrs786204726
23andMers786204726
23andMe allrs786204726
SNP Nexus

SNPshotrs786204726
SNPdbers786204726
MSV3drs786204726
GWAS Ctlgrs786204726
Max Magnitude0
ClinVar
Risk rs786204726(;)
Alt rs786204726(;)
Reference rs786204726(TGAC;TGAC)
Significance Other
Disease Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108235834_108235837delACTG
CLNSRC
CLNACC RCV000169561.2, RCV000236349.1,