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rs138603088

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs138603088(A;T)
Make rs138603088(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position36930783
GeneSAMHD1
is asnp
is mentioned by
dbSNPrs138603088
ebirs138603088
HLIrs138603088
Exacrs138603088
Varsomers138603088
Maprs138603088
PheGenIrs138603088
hapmaprs138603088
1000 genomesrs138603088
hgdprs138603088
ensemblrs138603088
gopubmedrs138603088
geneviewrs138603088
scholarrs138603088
googlers138603088
pharmgkbrs138603088
gwascentralrs138603088
openSNPrs138603088
23andMers138603088
23andMe allrs138603088
SNP Nexus

SNPshotrs138603088
SNPdbers138603088
MSV3drs138603088
GWAS Ctlgrs138603088
Max Magnitude0
ClinVar
Risk rs138603088(T;T)
Alt rs138603088(T;T)
Reference rs138603088(A;A)
Significance Pathogenic
Disease Aicardi Goutieres syndrome 5 Chilblain lupus 2
Variation info
Gene SAMHD1
CLNDBN Aicardi Goutieres syndrome 5 Chilblain lupus 2
Reversed 0
HGVS NC_000020.10:g.35559186A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023578.7, RCV000023579.5,