rs796053507

Orientation

plus

Stabilized

plus

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

Make rs796053507(-;-)

Make rs796053507(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

2088448

Gene	PKD1, TSC2

is a	snp
is	mentioned by
dbSNP	rs796053507
dbSNP (classic)	rs796053507
ClinGen	rs796053507
ebi	rs796053507
HLI	rs796053507
Exac	rs796053507
Gnomad	rs796053507
Varsome	rs796053507
LitVar	rs796053507
Map	rs796053507
PheGenI	rs796053507
Biobank	rs796053507
1000 genomes	rs796053507
hgdp	rs796053507
ensembl	rs796053507
geneview	rs796053507
scholar	rs796053507
google	rs796053507
pharmgkb	rs796053507
gwascentral	rs796053507
openSNP	rs796053507
23andMe	rs796053507
SNPshot	rs796053507
SNPdbe	rs796053507
MSV3d	rs796053507
GWAS Ctlg	rs796053507

Max Magnitude

0

ClinVar
Risk	rs796053507(-;-)
Alt	rs796053507(-;-)
Reference	Rs796053507(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TSC2 PKD1
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.2138449delC
CLNSRC
CLNACC	RCV000190064.1,