rs878853348

Orientation

plus

Stabilized

plus

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

Make rs878853348(-;-)

Make rs878853348(-;TTCC)

Make rs878853348(TTCC;TTCC)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

90679609

Gene

ADGRV1

is a	snp
is	mentioned by
dbSNP	rs878853348
dbSNP (classic)	rs878853348
ClinGen	rs878853348
ebi	rs878853348
HLI	rs878853348
Exac	rs878853348
Gnomad	rs878853348
Varsome	rs878853348
LitVar	rs878853348
Map	rs878853348
PheGenI	rs878853348
Biobank	rs878853348
1000 genomes	rs878853348
hgdp	rs878853348
ensembl	rs878853348
geneview	rs878853348
scholar	rs878853348
google	rs878853348
pharmgkb	rs878853348
gwascentral	rs878853348
openSNP	rs878853348
23andMe	rs878853348
SNPshot	rs878853348
SNPdbe	rs878853348
MSV3d	rs878853348
GWAS Ctlg	rs878853348

Max Magnitude

0

ClinVar
Risk	rs878853348(-;-)
Alt	rs878853348(-;-)
Reference	Rs878853348(CTTC;CTTC)
Significance	Probable-Pathogenic
Disease	Retinal dystrophy
Variation	info
Gene	GPR98 ADGRV1
CLNDBN	Retinal dystrophy
Reversed	0
HGVS	NC_000005.9:g.89975426_89975429delTTCC
CLNSRC
CLNACC	RCV000225506.1,