rs267606887

Orientation

minus

Stabilized

minus

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

Make rs267606887(A;G)

Make rs267606887(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11795158

Gene

MTHFR

is a	snp
is	mentioned by
dbSNP	rs267606887
dbSNP (classic)	rs267606887
ClinGen	rs267606887
ebi	rs267606887
HLI	rs267606887
Exac	rs267606887
Gnomad	rs267606887
Varsome	rs267606887
LitVar	rs267606887
Map	rs267606887
PheGenI	rs267606887
Biobank	rs267606887
1000 genomes	rs267606887
hgdp	rs267606887
ensembl	rs267606887
geneview	rs267606887
scholar	rs267606887
google	rs267606887
pharmgkb	rs267606887
gwascentral	rs267606887
openSNP	rs267606887
23andMe	rs267606887
SNPshot	rs267606887
SNPdbe	rs267606887
MSV3d	rs267606887
GWAS Ctlg	rs267606887

Max Magnitude

0

ClinVar
Risk	rs267606887(G;G)
Alt	rs267606887(G;G)
Reference	Rs267606887(A;A)
Significance	Pathogenic
Disease	Homocystinuria due to MTHFR deficiency
Variation	info
Gene	MTHFR
CLNDBN	Homocystinuria due to MTHFR deficiency
Reversed	1
HGVS	NC_000001.10:g.11855215T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000003700.2,