rs796051866

Orientation

plus

Stabilized

plus

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

Make rs796051866(-;-)

Make rs796051866(-;AAGTGCTGAAATC)

Make rs796051866(AAGTGCTGAAATC;AAGTGCTGAAATC)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

90642653

Gene

ADGRV1

is a	snp
is	mentioned by
dbSNP	rs796051866
dbSNP (classic)	rs796051866
ClinGen	rs796051866
ebi	rs796051866
HLI	rs796051866
Exac	rs796051866
Gnomad	rs796051866
Varsome	rs796051866
LitVar	rs796051866
Map	rs796051866
PheGenI	rs796051866
Biobank	rs796051866
1000 genomes	rs796051866
hgdp	rs796051866
ensembl	rs796051866
geneview	rs796051866
scholar	rs796051866
google	rs796051866
pharmgkb	rs796051866
gwascentral	rs796051866
openSNP	rs796051866
23andMe	rs796051866
SNPshot	rs796051866
SNPdbe	rs796051866
MSV3d	rs796051866
GWAS Ctlg	rs796051866

Max Magnitude

0

ClinVar
Risk	rs796051866(-;-)
Alt	rs796051866(-;-)
Reference	Rs796051866(CAAGTGCTGAAAT;CAAGTGCTGAAAT)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	ADGRV1 GPR98
CLNDBN	Usher syndrome, type 2C
Reversed	0
HGVS	NC_000005.9:g.89938470_89938482delAAGTGCTGAAATC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007206.6,