rs121909077

Orientation

minus

Stabilized

minus

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

Make rs121909077(C;T)

Make rs121909077(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

35500032

Gene

TULP1

is a	snp
is	mentioned by
dbSNP	rs121909077
dbSNP (classic)	rs121909077
ClinGen	rs121909077
ebi	rs121909077
HLI	rs121909077
Exac	rs121909077
Gnomad	rs121909077
Varsome	rs121909077
LitVar	rs121909077
Map	rs121909077
PheGenI	rs121909077
Biobank	rs121909077
1000 genomes	rs121909077
hgdp	rs121909077
ensembl	rs121909077
geneview	rs121909077
scholar	rs121909077
google	rs121909077
pharmgkb	rs121909077
gwascentral	rs121909077
openSNP	rs121909077
23andMe	rs121909077
SNPshot	rs121909077
SNPdbe	rs121909077
MSV3d	rs121909077
GWAS Ctlg	rs121909077

Max Magnitude

0

OMIM	602280
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121909077(T;T)
Alt	rs121909077(T;T)
Reference	Rs121909077(C;C)
Significance	Pathogenic
Disease	Retinitis pigmentosa 14
Variation	info
Gene	TULP1
CLNDBN	Retinitis pigmentosa 14
Reversed	1
HGVS	NC_000006.11:g.35467809G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007788.3,