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rs146365382

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs146365382(A;G)
Make rs146365382(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position197706499
GeneMARS2
is asnp
is mentioned by
dbSNPrs146365382
ebirs146365382
HLIrs146365382
Exacrs146365382
Varsomers146365382
Maprs146365382
PheGenIrs146365382
hapmaprs146365382
1000 genomesrs146365382
hgdprs146365382
ensemblrs146365382
gopubmedrs146365382
geneviewrs146365382
scholarrs146365382
googlers146365382
pharmgkbrs146365382
gwascentralrs146365382
openSNPrs146365382
23andMers146365382
23andMe allrs146365382
SNP Nexus

SNPshotrs146365382
SNPdbers146365382
MSV3drs146365382
GWAS Ctlgrs146365382
Max Magnitude0
ClinVar
Risk rs146365382(G;G)
Alt rs146365382(G;G)
Reference rs146365382(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MARS2
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.198571223A>G
CLNSRC
CLNACC RCV000195863.2,