rs767103817

Orientation

plus

Stabilized

plus

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

Make rs767103817(A;A)

Make rs767103817(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

119092407

Gene

HMBS

is a	snp
is	mentioned by
dbSNP	rs767103817
dbSNP (classic)	rs767103817
ClinGen	rs767103817
ebi	rs767103817
HLI	rs767103817
Exac	rs767103817
Gnomad	rs767103817
Varsome	rs767103817
LitVar	rs767103817
Map	rs767103817
PheGenI	rs767103817
Biobank	rs767103817
1000 genomes	rs767103817
hgdp	rs767103817
ensembl	rs767103817
geneview	rs767103817
scholar	rs767103817
google	rs767103817
pharmgkb	rs767103817
gwascentral	rs767103817
openSNP	rs767103817
23andMe	rs767103817
SNPshot	rs767103817
SNPdbe	rs767103817
MSV3d	rs767103817
GWAS Ctlg	rs767103817

Max Magnitude

0

ClinVar
Risk	rs767103817(A;A) rs767103817(T;T)
Alt	rs767103817(A;A) rs767103817(T;T)
Reference	Rs767103817(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HMBS
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.118963117G>A
CLNSRC
CLNACC	RCV000484759.1,