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rs77672568

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs77672568(-;-)
Make rs77672568(-;G)
Make rs77672568(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position12807213
GeneRNASEH2A
is asnp
is mentioned by
dbSNPrs77672568
ebirs77672568
HLIrs77672568
Exacrs77672568
Varsomers77672568
Maprs77672568
PheGenIrs77672568
hapmaprs77672568
1000 genomesrs77672568
hgdprs77672568
ensemblrs77672568
gopubmedrs77672568
geneviewrs77672568
scholarrs77672568
googlers77672568
pharmgkbrs77672568
gwascentralrs77672568
openSNPrs77672568
23andMers77672568
23andMe allrs77672568
SNP Nexus

SNPshotrs77672568
SNPdbers77672568
MSV3drs77672568
GWAS Ctlgrs77672568
Max Magnitude0
ClinVar
Risk rs77672568(G;G)
Alt rs77672568(G;G)
Reference rs77672568(;)
Significance Pathogenic
Disease Aicardi Goutieres syndrome 4
Variation info
Gene RNASEH2A
CLNDBN Aicardi Goutieres syndrome 4
Reversed 0
HGVS NC_000019.9:g.12918027dupG
CLNSRC ClinVar
CLNACC RCV000114337.2,