rs35648932

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs35648932(C;T)

Make rs35648932(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

109561798

Gene

MMAB

is a	snp
is	mentioned by
dbSNP	rs35648932
dbSNP (classic)	rs35648932
ClinGen	rs35648932
ebi	rs35648932
HLI	rs35648932
Exac	rs35648932
Gnomad	rs35648932
Varsome	rs35648932
LitVar	rs35648932
Map	rs35648932
PheGenI	rs35648932
Biobank	rs35648932
1000 genomes	rs35648932
hgdp	rs35648932
ensembl	rs35648932
geneview	rs35648932
scholar	rs35648932
google	rs35648932
pharmgkb	rs35648932
gwascentral	rs35648932
openSNP	rs35648932
23andMe	rs35648932
SNPshot	rs35648932
SNPdbe	rs35648932
MSV3d	rs35648932
GWAS Ctlg	rs35648932

Max Magnitude

0

ClinVar
Risk	rs35648932(T;T)
Alt	rs35648932(T;T)
Reference	Rs35648932(C;C)
Significance	Pathogenic
Disease	Methylmalonic aciduria cblB type not specified
Variation	info
Gene	MMAB
CLNDBN	Methylmalonic aciduria cblB type not specified
Reversed	0
HGVS	NC_000012.11:g.109999603C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000203394.1, RCV000482151.1,