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rs151079750

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151079750(A;A)
Make rs151079750(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position68936288
GeneIGHMBP2
is asnp
is mentioned by
dbSNPrs151079750
ebirs151079750
HLIrs151079750
Exacrs151079750
Varsomers151079750
Maprs151079750
PheGenIrs151079750
hapmaprs151079750
1000 genomesrs151079750
hgdprs151079750
ensemblrs151079750
gopubmedrs151079750
geneviewrs151079750
scholarrs151079750
googlers151079750
pharmgkbrs151079750
gwascentralrs151079750
openSNPrs151079750
23andMers151079750
23andMe allrs151079750
SNP Nexus

SNPshotrs151079750
SNPdbers151079750
MSV3drs151079750
GWAS Ctlgrs151079750
Max Magnitude0
ClinVar
Risk rs151079750(A;A)
Alt rs151079750(A;A)
Reference rs151079750(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene IGHMBP2
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.68703756G>A
CLNSRC
CLNACC RCV000224756.1,