rs587777809

Orientation

plus

Stabilized

plus

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

Make rs587777809(A;G)

Make rs587777809(G;G)

Reference

GRCh38 38.1/142

Chromosome

14

Position

88833691

Gene

TTC8

is a	snp
is	mentioned by
dbSNP	rs587777809
dbSNP (classic)	rs587777809
ClinGen	rs587777809
ebi	rs587777809
HLI	rs587777809
Exac	rs587777809
Gnomad	rs587777809
Varsome	rs587777809
LitVar	rs587777809
Map	rs587777809
PheGenI	rs587777809
Biobank	rs587777809
1000 genomes	rs587777809
hgdp	rs587777809
ensembl	rs587777809
geneview	rs587777809
scholar	rs587777809
google	rs587777809
pharmgkb	rs587777809
gwascentral	rs587777809
openSNP	rs587777809
23andMe	rs587777809
SNPshot	rs587777809
SNPdbe	rs587777809
MSV3d	rs587777809
GWAS Ctlg	rs587777809

Max Magnitude

0

ClinVar
Risk	rs587777809(G;G)
Alt	rs587777809(G;G)
Reference	Rs587777809(A;A)
Significance	Pathogenic
Disease	Retinitis pigmentosa 51
Variation	info
Gene	TTC8
CLNDBN	Retinitis pigmentosa 51
Reversed	0
HGVS	NC_000014.8:g.89300035A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002641.6,