rs796053515

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(I;I)	0	common genotype
(T;T)	0	common in clinvar

Make rs796053515(-;-)

Make rs796053515(-;T)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

2048647

Gene	NTHL1, TSC2

is a	snp
is	mentioned by
dbSNP	rs796053515
dbSNP (classic)	rs796053515
ClinGen	rs796053515
ebi	rs796053515
HLI	rs796053515
Exac	rs796053515
Gnomad	rs796053515
Varsome	rs796053515
LitVar	rs796053515
Map	rs796053515
PheGenI	rs796053515
Biobank	rs796053515
1000 genomes	rs796053515
hgdp	rs796053515
ensembl	rs796053515
geneview	rs796053515
scholar	rs796053515
google	rs796053515
pharmgkb	rs796053515
gwascentral	rs796053515
openSNP	rs796053515
23andMe	rs796053515
SNPshot	rs796053515
SNPdbe	rs796053515
MSV3d	rs796053515
GWAS Ctlg	rs796053515

Max Magnitude

0

ClinVar
Risk	rs796053515(-;-)
Alt	rs796053515(-;-)
Reference	Rs796053515(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	NTHL1 TSC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.2098648delT
CLNSRC
CLNACC	RCV000190084.1,