rs587777808

Orientation

plus

Stabilized

plus

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

Make rs587777808(A;A)

Make rs587777808(A;G)

Reference

GRCh38 38.1/142

Chromosome

14

Position

88843851

Gene

TTC8

is a	snp
is	mentioned by
dbSNP	rs587777808
dbSNP (classic)	rs587777808
ClinGen	rs587777808
ebi	rs587777808
HLI	rs587777808
Exac	rs587777808
Gnomad	rs587777808
Varsome	rs587777808
LitVar	rs587777808
Map	rs587777808
PheGenI	rs587777808
Biobank	rs587777808
1000 genomes	rs587777808
hgdp	rs587777808
ensembl	rs587777808
geneview	rs587777808
scholar	rs587777808
google	rs587777808
pharmgkb	rs587777808
gwascentral	rs587777808
openSNP	rs587777808
23andMe	rs587777808
SNPshot	rs587777808
SNPdbe	rs587777808
MSV3d	rs587777808
GWAS Ctlg	rs587777808

Max Magnitude

0

ClinVar
Risk	rs587777808(A;A)
Alt	rs587777808(A;A)
Reference	Rs587777808(G;G)
Significance	Pathogenic
Disease	Bardet-Biedl syndrome 8
Variation	info
Gene	TTC8
CLNDBN	Bardet-Biedl syndrome 8
Reversed	0
HGVS	NC_000014.8:g.89310195G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002640.3,