rs797044445

Orientation

plus

Stabilized

plus

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

Make rs797044445(-;A)

Make rs797044445(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

236894532

Gene

MTR

is a	snp
is	mentioned by
dbSNP	rs797044445
dbSNP (classic)	rs797044445
ClinGen	rs797044445
ebi	rs797044445
HLI	rs797044445
Exac	rs797044445
Gnomad	rs797044445
Varsome	rs797044445
LitVar	rs797044445
Map	rs797044445
PheGenI	rs797044445
Biobank	rs797044445
1000 genomes	rs797044445
hgdp	rs797044445
ensembl	rs797044445
geneview	rs797044445
scholar	rs797044445
google	rs797044445
pharmgkb	rs797044445
gwascentral	rs797044445
openSNP	rs797044445
23andMe	rs797044445
SNPshot	rs797044445
SNPdbe	rs797044445
MSV3d	rs797044445
GWAS Ctlg	rs797044445

Max Magnitude

0

ClinVar
Risk	rs797044445(A;A)
Alt	rs797044445(A;A)
Reference	Rs797044445(-;-)
Significance	Pathogenic
Disease	METHYLCOBALAMIN DEFICIENCY
Variation	info
Gene	MTR
CLNDBN	METHYLCOBALAMIN DEFICIENCY, cblG TYPE
Reversed	0
HGVS	NC_000001.10:g.237057832dupA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015354.27,