rs1057519360

Orientation

minus

Stabilized

minus

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

Make rs1057519360(C;T)

Make rs1057519360(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

11801220

Gene

MTHFR

is a	snp
is	mentioned by
dbSNP	rs1057519360
dbSNP (classic)	rs1057519360
ClinGen	rs1057519360
ebi	rs1057519360
HLI	rs1057519360
Exac	rs1057519360
Gnomad	rs1057519360
Varsome	rs1057519360
LitVar	rs1057519360
Map	rs1057519360
PheGenI	rs1057519360
Biobank	rs1057519360
1000 genomes	rs1057519360
hgdp	rs1057519360
ensembl	rs1057519360
geneview	rs1057519360
scholar	rs1057519360
google	rs1057519360
pharmgkb	rs1057519360
gwascentral	rs1057519360
openSNP	rs1057519360
23andMe	rs1057519360
SNPshot	rs1057519360
SNPdbe	rs1057519360
MSV3d	rs1057519360
GWAS Ctlg	rs1057519360

Max Magnitude

0

ClinVar
Risk	rs1057519360(T;T)
Alt	rs1057519360(T;T)
Reference	Rs1057519360(C;C)
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.11861277G>A
CLNSRC
CLNACC	RCV000416816.1,