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rs398123455

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123455(A;A)
Make rs398123455(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position12652270
GeneMAN2B1
is asnp
is mentioned by
dbSNPrs398123455
ebirs398123455
HLIrs398123455
Exacrs398123455
Varsomers398123455
Maprs398123455
PheGenIrs398123455
hapmaprs398123455
1000 genomesrs398123455
hgdprs398123455
ensemblrs398123455
gopubmedrs398123455
geneviewrs398123455
scholarrs398123455
googlers398123455
pharmgkbrs398123455
gwascentralrs398123455
openSNPrs398123455
23andMers398123455
23andMe allrs398123455
SNP Nexus

SNPshotrs398123455
SNPdbers398123455
MSV3drs398123455
GWAS Ctlgrs398123455
Max Magnitude0
ClinVar
Risk rs398123455(A;A)
Alt rs398123455(A;A)
Reference rs398123455(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MAN2B1
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.12763084C>T
CLNSRC HGMD
CLNACC RCV000079075.4,