rs1057518098

Orientation

minus

Stabilized

minus

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

Make rs1057518098(-;TAAT)

Make rs1057518098(TAAT;TAAT)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

86643827

Gene

CNGB3

is a	snp
is	mentioned by
dbSNP	rs1057518098
dbSNP (classic)	rs1057518098
ClinGen	rs1057518098
ebi	rs1057518098
HLI	rs1057518098
Exac	rs1057518098
Gnomad	rs1057518098
Varsome	rs1057518098
LitVar	rs1057518098
Map	rs1057518098
PheGenI	rs1057518098
Biobank	rs1057518098
1000 genomes	rs1057518098
hgdp	rs1057518098
ensembl	rs1057518098
geneview	rs1057518098
scholar	rs1057518098
google	rs1057518098
pharmgkb	rs1057518098
gwascentral	rs1057518098
openSNP	rs1057518098
23andMe	rs1057518098
SNPshot	rs1057518098
SNPdbe	rs1057518098
MSV3d	rs1057518098
GWAS Ctlg	rs1057518098

Max Magnitude

0

ClinVar
Risk	rs1057518098(TAAT;TAAT)
Alt	rs1057518098(TAAT;TAAT)
Reference	Rs1057518098(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CNGB3
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.87656056_87656059dupATTA
CLNSRC
CLNACC	RCV000412821.1,