rs876661297

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AAG;AAG)	0	common in clinvar
(AGA;AGA)	0	common in clinvar

Make rs876661297(-;-)

Make rs876661297(-;AAG)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

3129168

Gene	LOC107986006, TRNT1

is a	snp
is	mentioned by
dbSNP	rs876661297
dbSNP (classic)	rs876661297
ClinGen	rs876661297
ebi	rs876661297
HLI	rs876661297
Exac	rs876661297
Gnomad	rs876661297
Varsome	rs876661297
LitVar	rs876661297
Map	rs876661297
PheGenI	rs876661297
Biobank	rs876661297
1000 genomes	rs876661297
hgdp	rs876661297
ensembl	rs876661297
geneview	rs876661297
scholar	rs876661297
google	rs876661297
pharmgkb	rs876661297
gwascentral	rs876661297
openSNP	rs876661297
23andMe	rs876661297
SNPshot	rs876661297
SNPdbe	rs876661297
MSV3d	rs876661297
GWAS Ctlg	rs876661297

Max Magnitude

0

ClinVar
Risk	rs876661297(-;-) Rs876661297(AGA;AGA)
Alt	rs876661297(-;-) Rs876661297(AGA;AGA)
Reference	Rs876661297(AAG;AAG)
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.3170852_3170854delAAG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000223678.1,