rs777661576

Orientation

plus

Stabilized

plus

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

Make rs777661576(C;T)

Make rs777661576(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

11790916

Gene

MTHFR

is a	snp
is	mentioned by
dbSNP	rs777661576
dbSNP (classic)	rs777661576
ClinGen	rs777661576
ebi	rs777661576
HLI	rs777661576
Exac	rs777661576
Gnomad	rs777661576
Varsome	rs777661576
LitVar	rs777661576
Map	rs777661576
PheGenI	rs777661576
Biobank	rs777661576
1000 genomes	rs777661576
hgdp	rs777661576
ensembl	rs777661576
geneview	rs777661576
scholar	rs777661576
google	rs777661576
pharmgkb	rs777661576
gwascentral	rs777661576
openSNP	rs777661576
23andMe	rs777661576
SNPshot	rs777661576
SNPdbe	rs777661576
MSV3d	rs777661576
GWAS Ctlg	rs777661576

Max Magnitude

0

ClinVar
Risk	rs777661576(T;T)
Alt	rs777661576(T;T)
Reference	Rs777661576(C;C)
Significance	Pathogenic
Disease	Homocysteinemia due to MTHFR deficiency
Variation	info
Gene	MTHFR
CLNDBN	Homocysteinemia due to MTHFR deficiency
Reversed	0
HGVS	NC_000001.10:g.11850973C>T
CLNSRC
CLNACC	RCV000167621.1,