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rs756195708

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756195708(C;T)
Make rs756195708(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position109561040
GeneMMAB
is asnp
is mentioned by
dbSNPrs756195708
ebirs756195708
HLIrs756195708
Exacrs756195708
Varsomers756195708
Maprs756195708
PheGenIrs756195708
hapmaprs756195708
1000 genomesrs756195708
hgdprs756195708
ensemblrs756195708
gopubmedrs756195708
geneviewrs756195708
scholarrs756195708
googlers756195708
pharmgkbrs756195708
gwascentralrs756195708
openSNPrs756195708
23andMers756195708
23andMe allrs756195708
SNP Nexus

SNPshotrs756195708
SNPdbers756195708
MSV3drs756195708
GWAS Ctlgrs756195708
Max Magnitude0
ClinVar
Risk rs756195708(T;T)
Alt rs756195708(T;T)
Reference rs756195708(C;C)
Significance Pathogenic
Disease Methylmalonic aciduria cblB type
Variation info
Gene MMAB
CLNDBN Methylmalonic aciduria cblB type
Reversed 0
HGVS NC_000012.11:g.109998845C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000202574.2,