rs796051998

Orientation

plus

Stabilized

plus

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

Make rs796051998(-;-)

Make rs796051998(-;TAC)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

45508323

Gene

MMACHC

is a	snp
is	mentioned by
dbSNP	rs796051998
dbSNP (classic)	rs796051998
ClinGen	rs796051998
ebi	rs796051998
HLI	rs796051998
Exac	rs796051998
Gnomad	rs796051998
Varsome	rs796051998
LitVar	rs796051998
Map	rs796051998
PheGenI	rs796051998
Biobank	rs796051998
1000 genomes	rs796051998
hgdp	rs796051998
ensembl	rs796051998
geneview	rs796051998
scholar	rs796051998
google	rs796051998
pharmgkb	rs796051998
gwascentral	rs796051998
openSNP	rs796051998
23andMe	rs796051998
SNPshot	rs796051998
SNPdbe	rs796051998
MSV3d	rs796051998
GWAS Ctlg	rs796051998

Max Magnitude

0

ClinVar
Risk	rs796051998(-;-)
Alt	rs796051998(-;-)
Reference	Rs796051998(TAC;TAC)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MMACHC
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.45973995_45973997delTAC
CLNSRC
CLNACC	RCV000186033.1,