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rs369587937

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369587937(G;T)
Make rs369587937(T;T)
ReferenceGRCh38 38.1/142
Chromosome20
Position36905450
GeneSAMHD1
is asnp
is mentioned by
dbSNPrs369587937
ebirs369587937
HLIrs369587937
Exacrs369587937
Varsomers369587937
Maprs369587937
PheGenIrs369587937
hapmaprs369587937
1000 genomesrs369587937
hgdprs369587937
ensemblrs369587937
gopubmedrs369587937
geneviewrs369587937
scholarrs369587937
googlers369587937
pharmgkbrs369587937
gwascentralrs369587937
openSNPrs369587937
23andMers369587937
23andMe allrs369587937
SNP Nexus

SNPshotrs369587937
SNPdbers369587937
MSV3drs369587937
GWAS Ctlgrs369587937
Max Magnitude0
ClinVar
Risk rs369587937(A,T;A,T)
Alt rs369587937(A,T;A,T)
Reference rs369587937(G;G)
Significance Pathogenic
Disease Aicardi Goutieres syndrome 5
Variation info
Gene SAMHD1
CLNDBN Aicardi Goutieres syndrome 5
Reversed 0
HGVS NC_000020.10:g.35533853G>A
CLNSRC ClinVar
CLNACC RCV000114347.2,