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rs796051856

From SNPedia

Orientationplus
Make rs796051856(-;-)
Make rs796051856(-;CTTAGG)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108329210
GeneATM
is asnp
is mentioned by
dbSNPrs796051856
ebirs796051856
HLIrs796051856
Exacrs796051856
Varsomers796051856
Maprs796051856
PheGenIrs796051856
hapmaprs796051856
1000 genomesrs796051856
hgdprs796051856
ensemblrs796051856
gopubmedrs796051856
geneviewrs796051856
scholarrs796051856
googlers796051856
pharmgkbrs796051856
gwascentralrs796051856
openSNPrs796051856
23andMers796051856
23andMe allrs796051856
SNP Nexus

SNPshotrs796051856
SNPdbers796051856
MSV3drs796051856
GWAS Ctlgrs796051856
Max Magnitude
ClinVar
Risk rs796051856(;)
Alt rs796051856(;)
Reference rs796051856(CTTAGG;CTTAGG)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108199937_108199942delCTTAGG
CLNSRC OMIM Allelic Variant
CLNACC RCV000003156.3,