rs367585605

Orientation

plus

Stabilized

plus

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

Make rs367585605(C;T)

Make rs367585605(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

11794385

Gene

MTHFR

is a	snp
is	mentioned by
dbSNP	rs367585605
dbSNP (classic)	rs367585605
ClinGen	rs367585605
ebi	rs367585605
HLI	rs367585605
Exac	rs367585605
Gnomad	rs367585605
Varsome	rs367585605
LitVar	rs367585605
Map	rs367585605
PheGenI	rs367585605
Biobank	rs367585605
1000 genomes	rs367585605
hgdp	rs367585605
ensembl	rs367585605
geneview	rs367585605
scholar	rs367585605
google	rs367585605
pharmgkb	rs367585605
gwascentral	rs367585605
openSNP	rs367585605
23andMe	rs367585605
SNPshot	rs367585605
SNPdbe	rs367585605
MSV3d	rs367585605
GWAS Ctlg	rs367585605

Max Magnitude

0

ClinVar
Risk	rs367585605(T;T)
Alt	rs367585605(T;T)
Reference	Rs367585605(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.11854442C>T
CLNSRC
CLNACC	RCV000167613.1,