rs1057521126

Orientation

plus

Stabilized

plus

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

Make rs1057521126(A;A)

Make rs1057521126(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

119092785

Gene

HMBS

is a	snp
is	mentioned by
dbSNP	rs1057521126
dbSNP (classic)	rs1057521126
ClinGen	rs1057521126
ebi	rs1057521126
HLI	rs1057521126
Exac	rs1057521126
Gnomad	rs1057521126
Varsome	rs1057521126
LitVar	rs1057521126
Map	rs1057521126
PheGenI	rs1057521126
Biobank	rs1057521126
1000 genomes	rs1057521126
hgdp	rs1057521126
ensembl	rs1057521126
geneview	rs1057521126
scholar	rs1057521126
google	rs1057521126
pharmgkb	rs1057521126
gwascentral	rs1057521126
openSNP	rs1057521126
23andMe	rs1057521126
SNPshot	rs1057521126
SNPdbe	rs1057521126
MSV3d	rs1057521126
GWAS Ctlg	rs1057521126

Max Magnitude

0

ClinVar
Risk	rs1057521126(A;A)
Alt	rs1057521126(A;A)
Reference	Rs1057521126(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HMBS
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.118963495G>A
CLNSRC
CLNACC	RCV000430573.1,