rs796051997

Orientation

plus

Stabilized

plus

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

Make rs796051997(A;A)

Make rs796051997(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

45508966

Gene

MMACHC

is a	snp
is	mentioned by
dbSNP	rs796051997
dbSNP (classic)	rs796051997
ClinGen	rs796051997
ebi	rs796051997
HLI	rs796051997
Exac	rs796051997
Gnomad	rs796051997
Varsome	rs796051997
LitVar	rs796051997
Map	rs796051997
PheGenI	rs796051997
Biobank	rs796051997
1000 genomes	rs796051997
hgdp	rs796051997
ensembl	rs796051997
geneview	rs796051997
scholar	rs796051997
google	rs796051997
pharmgkb	rs796051997
gwascentral	rs796051997
openSNP	rs796051997
23andMe	rs796051997
SNPshot	rs796051997
SNPdbe	rs796051997
MSV3d	rs796051997
GWAS Ctlg	rs796051997

Max Magnitude

0

ClinVar
Risk	rs796051997(A;A)
Alt	rs796051997(A;A)
Reference	Rs796051997(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MMACHC
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.45974638G>A
CLNSRC
CLNACC	RCV000186031.1,