rs786205058

Orientation

minus

Stabilized

minus

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

Make rs786205058(A;A)

Make rs786205058(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

22

Position

37073531

Gene

TMPRSS6

is a	snp
is	mentioned by
dbSNP	rs786205058
dbSNP (classic)	rs786205058
ClinGen	rs786205058
ebi	rs786205058
HLI	rs786205058
Exac	rs786205058
Gnomad	rs786205058
Varsome	rs786205058
LitVar	rs786205058
Map	rs786205058
PheGenI	rs786205058
Biobank	rs786205058
1000 genomes	rs786205058
hgdp	rs786205058
ensembl	rs786205058
geneview	rs786205058
scholar	rs786205058
google	rs786205058
pharmgkb	rs786205058
gwascentral	rs786205058
openSNP	rs786205058
23andMe	rs786205058
SNPshot	rs786205058
SNPdbe	rs786205058
MSV3d	rs786205058
GWAS Ctlg	rs786205058

Max Magnitude

0

ClinVar
Risk	rs786205058(A;A)
Alt	rs786205058(A;A)
Reference	Rs786205058(G;G)
Significance	Pathogenic
Disease	Microcytic anemia
Variation	info
Gene	TMPRSS6
CLNDBN	Microcytic anemia
Reversed	1
HGVS	NC_000022.10:g.37469571C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001466.4,