rs121434586

Orientation

minus

Stabilized

minus

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

Make rs121434586(C;T)

Make rs121434586(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

49026719

Gene

IMPDH2

is a	snp
is	mentioned by
dbSNP	rs121434586
dbSNP (classic)	rs121434586
ClinGen	rs121434586
ebi	rs121434586
HLI	rs121434586
Exac	rs121434586
Gnomad	rs121434586
Varsome	rs121434586
LitVar	rs121434586
Map	rs121434586
PheGenI	rs121434586
Biobank	rs121434586
1000 genomes	rs121434586
hgdp	rs121434586
ensembl	rs121434586
geneview	rs121434586
scholar	rs121434586
google	rs121434586
pharmgkb	rs121434586
gwascentral	rs121434586
openSNP	rs121434586
23andMe	rs121434586
SNPshot	rs121434586
SNPdbe	rs121434586
MSV3d	rs121434586
GWAS Ctlg	rs121434586

Max Magnitude

0

OMIM	146691
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121434586(T;T)
Alt	rs121434586(T;T)
Reference	Rs121434586(C;C)
Significance	Other
Disease	Impdh2 enzyme activity
Variation	info
Gene	IMPDH2
CLNDBN	Impdh2 enzyme activity, variation in
Reversed	1
HGVS	NC_000003.11:g.49064152G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015958.26,