rs876661299

Orientation

plus

Stabilized

plus

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

Make rs876661299(C;C)

Make rs876661299(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

3146404

Gene

TRNT1

is a	snp
is	mentioned by
dbSNP	rs876661299
dbSNP (classic)	rs876661299
ClinGen	rs876661299
ebi	rs876661299
HLI	rs876661299
Exac	rs876661299
Gnomad	rs876661299
Varsome	rs876661299
LitVar	rs876661299
Map	rs876661299
PheGenI	rs876661299
Biobank	rs876661299
1000 genomes	rs876661299
hgdp	rs876661299
ensembl	rs876661299
geneview	rs876661299
scholar	rs876661299
google	rs876661299
pharmgkb	rs876661299
gwascentral	rs876661299
openSNP	rs876661299
23andMe	rs876661299
SNPshot	rs876661299
SNPdbe	rs876661299
MSV3d	rs876661299
GWAS Ctlg	rs876661299

Max Magnitude

0

ClinVar
Risk	rs876661299(C;C)
Alt	rs876661299(C;C)
Reference	Rs876661299(T;T)
Significance	Pathogenic
Disease	Retinitis pigmentosa and erythrocytic microcytosis
Variation	info
Gene	TRNT1
CLNDBN	Retinitis pigmentosa and erythrocytic microcytosis
Reversed	0
HGVS	NC_000003.11:g.3188088T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000223676.1,