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rs398123457

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123457(C;C)
Make rs398123457(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position12649134
GeneMAN2B1
is asnp
is mentioned by
dbSNPrs398123457
ebirs398123457
HLIrs398123457
Exacrs398123457
Varsomers398123457
Maprs398123457
PheGenIrs398123457
hapmaprs398123457
1000 genomesrs398123457
hgdprs398123457
ensemblrs398123457
gopubmedrs398123457
geneviewrs398123457
scholarrs398123457
googlers398123457
pharmgkbrs398123457
gwascentralrs398123457
openSNPrs398123457
23andMers398123457
23andMe allrs398123457
SNP Nexus

SNPshotrs398123457
SNPdbers398123457
MSV3drs398123457
GWAS Ctlgrs398123457
Max Magnitude0
ClinVar
Risk rs398123457(C;C)
Alt rs398123457(C;C)
Reference rs398123457(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MAN2B1
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.12759948A>G
CLNSRC ClinVar
CLNACC RCV000079077.4,