rs886037911

Orientation

minus

Stabilized

minus

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

Make rs886037911(C;C)

Make rs886037911(C;G)

Reference

GRCh38.p7 38.3/149

Chromosome

7

Position

128398504

Gene

IMPDH1

is a	snp
is	mentioned by
dbSNP	rs886037911
dbSNP (classic)	rs886037911
ClinGen	rs886037911
ebi	rs886037911
HLI	rs886037911
Exac	rs886037911
Gnomad	rs886037911
Varsome	rs886037911
LitVar	rs886037911
Map	rs886037911
PheGenI	rs886037911
Biobank	rs886037911
1000 genomes	rs886037911
hgdp	rs886037911
ensembl	rs886037911
geneview	rs886037911
scholar	rs886037911
google	rs886037911
pharmgkb	rs886037911
gwascentral	rs886037911
openSNP	rs886037911
23andMe	rs886037911
SNPshot	rs886037911
SNPdbe	rs886037911
MSV3d	rs886037911
GWAS Ctlg	rs886037911

Max Magnitude

0

ClinVar
Risk	rs886037911(C;C)
Alt	rs886037911(C;C)
Reference	Rs886037911(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 10
Variation	info
Gene	IMPDH1
CLNDBN	Retinitis pigmentosa 10
Reversed	1
HGVS	NC_000007.13:g.128038558C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000240659.1,