Have questions? Visit https://www.reddit.com/r/SNPedia

rs78762691

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs78762691(-;-)
Make rs78762691(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position48467052
GeneTREX1
is asnp
is mentioned by
dbSNPrs78762691
ebirs78762691
HLIrs78762691
Exacrs78762691
Varsomers78762691
Maprs78762691
PheGenIrs78762691
hapmaprs78762691
1000 genomesrs78762691
hgdprs78762691
ensemblrs78762691
gopubmedrs78762691
geneviewrs78762691
scholarrs78762691
googlers78762691
pharmgkbrs78762691
gwascentralrs78762691
openSNPrs78762691
23andMers78762691
23andMe allrs78762691
SNP Nexus

SNPshotrs78762691
SNPdbers78762691
MSV3drs78762691
GWAS Ctlgrs78762691
Max Magnitude0
ClinVar
Risk rs78762691(;)
Alt rs78762691(;)
Reference rs78762691(C;C)
Significance Pathogenic
Disease Aicardi Goutieres syndrome 1
Variation info
Gene ATRIP TREX1
CLNDBN Aicardi Goutieres syndrome 1
Reversed 0
HGVS NC_000003.11:g.48508451delC
CLNSRC ClinVar
CLNACC RCV000114327.2,