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rs764273304

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs764273304(C;C)
Make rs764273304(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position131583398
GeneARG1, MED23
is asnp
is mentioned by
dbSNPrs764273304
dbSNP (classic)rs764273304
ClinGenrs764273304
ebirs764273304
HLIrs764273304
Exacrs764273304
Gnomadrs764273304
Varsomers764273304
LitVarrs764273304
Maprs764273304
PheGenIrs764273304
Biobankrs764273304
1000 genomesrs764273304
hgdprs764273304
ensemblrs764273304
geneviewrs764273304
scholarrs764273304
googlers764273304
pharmgkbrs764273304
gwascentralrs764273304
openSNPrs764273304
23andMers764273304
23andMe allrs764273304
SNPshotrs764273304
SNPdbers764273304
MSV3drs764273304
GWAS Ctlgrs764273304
Max Magnitude0
ClinVar
Risk rs764273304(A;A) rs764273304(C;C)
Alt rs764273304(A;A) rs764273304(C;C)
Reference Rs764273304(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MED23 ARG1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.131904538G>A
CLNSRC
CLNACC RCV000489823.1,