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rs796051923

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796051923(-;-)
Make rs796051923(-;G)
Make rs796051923(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position131579252
GeneARG1, MED23
is asnp
is mentioned by
dbSNPrs796051923
ebirs796051923
HLIrs796051923
Exacrs796051923
Varsomers796051923
Maprs796051923
PheGenIrs796051923
hapmaprs796051923
1000 genomesrs796051923
hgdprs796051923
ensemblrs796051923
gopubmedrs796051923
geneviewrs796051923
scholarrs796051923
googlers796051923
pharmgkbrs796051923
gwascentralrs796051923
openSNPrs796051923
23andMers796051923
23andMe allrs796051923
SNP Nexus

SNPshotrs796051923
SNPdbers796051923
MSV3drs796051923
GWAS Ctlgrs796051923
Max Magnitude0
ClinVar
Risk rs796051923(G;G)
Alt rs796051923(G;G)
Reference rs796051923(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MED23 ARG1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.131900392dupG
CLNSRC
CLNACC RCV000185755.1,