rs875989821

Orientation

plus

Stabilized

plus

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

Make rs875989821(-;-)

Make rs875989821(-;TG)

Make rs875989821(TG;TG)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

46702736

Gene

ZNF408

is a	snp
is	mentioned by
dbSNP	rs875989821
dbSNP (classic)	rs875989821
ClinGen	rs875989821
ebi	rs875989821
HLI	rs875989821
Exac	rs875989821
Gnomad	rs875989821
Varsome	rs875989821
LitVar	rs875989821
Map	rs875989821
PheGenI	rs875989821
Biobank	rs875989821
1000 genomes	rs875989821
hgdp	rs875989821
ensembl	rs875989821
geneview	rs875989821
scholar	rs875989821
google	rs875989821
pharmgkb	rs875989821
gwascentral	rs875989821
openSNP	rs875989821
23andMe	rs875989821
SNPshot	rs875989821
SNPdbe	rs875989821
MSV3d	rs875989821
GWAS Ctlg	rs875989821

Max Magnitude

0

ClinVar
Risk	rs875989821(-;-)
Alt	rs875989821(-;-)
Reference	Rs875989821(GT;GT)
Significance	Pathogenic
Disease	Retinitis pigmentosa 72
Variation	info
Gene	ZNF408
CLNDBN	Retinitis pigmentosa 72
Reversed	0
HGVS	NC_000011.9:g.46724286_46724287delTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000186511.2,