rs765799472

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	Carrier of a methylmalonic aciduria type cblA mutation

Make rs765799472(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

145639203

Gene

MMAA

is a	snp
is	mentioned by
dbSNP	rs765799472
dbSNP (classic)	rs765799472
ClinGen	rs765799472
ebi	rs765799472
HLI	rs765799472
Exac	rs765799472
Gnomad	rs765799472
Varsome	rs765799472
LitVar	rs765799472
Map	rs765799472
PheGenI	rs765799472
Biobank	rs765799472
1000 genomes	rs765799472
hgdp	rs765799472
ensembl	rs765799472
geneview	rs765799472
scholar	rs765799472
google	rs765799472
pharmgkb	rs765799472
gwascentral	rs765799472
openSNP	rs765799472
23andMe	rs765799472
SNPshot	rs765799472
SNPdbe	rs765799472
MSV3d	rs765799472
GWAS Ctlg	rs765799472

Max Magnitude

3

ClinVar
Risk	rs765799472(T;T)
Alt	rs765799472(T;T)
Reference	Rs765799472(C;C)
Significance	Pathogenic
Disease	Methylmalonic aciduria cblA type not provided
Variation	info
Gene	MMAA
CLNDBN	Methylmalonic aciduria cblA type not provided
Reversed	0
HGVS	NC_000004.11:g.146560355C>T
CLNSRC
CLNACC	RCV000203329.1, RCV000488986.1,