rs1060499676

Orientation

plus

Stabilized

plus

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

Make rs1060499676(C;G)

Make rs1060499676(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2088234

Gene	PKD1, TSC2

is a	snp
is	mentioned by
dbSNP	rs1060499676
dbSNP (classic)	rs1060499676
ClinGen	rs1060499676
ebi	rs1060499676
HLI	rs1060499676
Exac	rs1060499676
Gnomad	rs1060499676
Varsome	rs1060499676
LitVar	rs1060499676
Map	rs1060499676
PheGenI	rs1060499676
Biobank	rs1060499676
1000 genomes	rs1060499676
hgdp	rs1060499676
ensembl	rs1060499676
geneview	rs1060499676
scholar	rs1060499676
google	rs1060499676
pharmgkb	rs1060499676
gwascentral	rs1060499676
openSNP	rs1060499676
23andMe	rs1060499676
SNPshot	rs1060499676
SNPdbe	rs1060499676
MSV3d	rs1060499676
GWAS Ctlg	rs1060499676

Max Magnitude

0

ClinVar
Risk	rs1060499676(G;G)
Alt	rs1060499676(G;G)
Reference	Rs1060499676(C;C)
Significance	Pathogenic
Disease	Tuberous sclerosis 2
Variation	info
Gene	TSC2 PKD1
CLNDBN	Tuberous sclerosis 2
Reversed	0
HGVS	NC_000016.9:g.2138235C>G
CLNSRC
CLNACC	RCV000449506.1,