rs121909073

Orientation

minus

Stabilized

minus

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

Make rs121909073(C;C)

Make rs121909073(C;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

35503623

Gene

TULP1

is a	snp
is	mentioned by
dbSNP	rs121909073
dbSNP (classic)	rs121909073
ClinGen	rs121909073
ebi	rs121909073
HLI	rs121909073
Exac	rs121909073
Gnomad	rs121909073
Varsome	rs121909073
LitVar	rs121909073
Map	rs121909073
PheGenI	rs121909073
Biobank	rs121909073
1000 genomes	rs121909073
hgdp	rs121909073
ensembl	rs121909073
geneview	rs121909073
scholar	rs121909073
google	rs121909073
pharmgkb	rs121909073
gwascentral	rs121909073
openSNP	rs121909073
23andMe	rs121909073
SNPshot	rs121909073
SNPdbe	rs121909073
MSV3d	rs121909073
GWAS Ctlg	rs121909073

Max Magnitude

0

OMIM	602280
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909073(C;C)
Alt	rs121909073(C;C)
Reference	Rs121909073(G;G)
Significance	Pathogenic
Disease	Retinitis pigmentosa 14 not provided
Variation	info
Gene	TULP1
CLNDBN	Retinitis pigmentosa 14 not provided
Reversed	1
HGVS	NC_000006.11:g.35471400C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007782.4, RCV000086066.1,