rs786204018

Orientation

minus

Stabilized

minus

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

Make rs786204018(G;T)

Make rs786204018(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

11796222

Gene

MTHFR

is a	snp
is	mentioned by
dbSNP	rs786204018
dbSNP (classic)	rs786204018
ClinGen	rs786204018
ebi	rs786204018
HLI	rs786204018
Exac	rs786204018
Gnomad	rs786204018
Varsome	rs786204018
LitVar	rs786204018
Map	rs786204018
PheGenI	rs786204018
Biobank	rs786204018
1000 genomes	rs786204018
hgdp	rs786204018
ensembl	rs786204018
geneview	rs786204018
scholar	rs786204018
google	rs786204018
pharmgkb	rs786204018
gwascentral	rs786204018
openSNP	rs786204018
23andMe	rs786204018
SNPshot	rs786204018
SNPdbe	rs786204018
MSV3d	rs786204018
GWAS Ctlg	rs786204018

Max Magnitude

0

ClinVar
Risk	rs786204018(T;T)
Alt	rs786204018(T;T)
Reference	Rs786204018(G;G)
Significance	Pathogenic
Disease	Homocysteinemia due to MTHFR deficiency
Variation	info
Gene	MTHFR
CLNDBN	Homocysteinemia due to MTHFR deficiency
Reversed	1
HGVS	NC_000001.10:g.11856279C>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000167602.1,