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rs369035155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369035155(C;T)
Make rs369035155(T;T)
ReferenceGRCh38 38.1/142
Chromosome20
Position36935110
GeneSAMHD1
is asnp
is mentioned by
dbSNPrs369035155
ebirs369035155
HLIrs369035155
Exacrs369035155
Varsomers369035155
Maprs369035155
PheGenIrs369035155
hapmaprs369035155
1000 genomesrs369035155
hgdprs369035155
ensemblrs369035155
gopubmedrs369035155
geneviewrs369035155
scholarrs369035155
googlers369035155
pharmgkbrs369035155
gwascentralrs369035155
openSNPrs369035155
23andMers369035155
23andMe allrs369035155
SNP Nexus

SNPshotrs369035155
SNPdbers369035155
MSV3drs369035155
GWAS Ctlgrs369035155
Max Magnitude0
ClinVar
Risk rs369035155(T;T)
Alt rs369035155(T;T)
Reference rs369035155(C;C)
Significance Pathogenic
Disease Aicardi Goutieres syndrome 5
Variation info
Gene SAMHD1
CLNDBN Aicardi Goutieres syndrome 5
Reversed 0
HGVS NC_000020.10:g.35563513C>T
CLNSRC ClinVar
CLNACC RCV000114352.2,