rs1064793853

Orientation

plus

Stabilized

plus

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

Chromosome

16

Position

2048746

Gene	NTHL1, TSC2

is a	snp
is	mentioned by
dbSNP	rs1064793853
dbSNP (classic)	rs1064793853
ClinGen	rs1064793853
ebi	rs1064793853
HLI	rs1064793853
Exac	rs1064793853
Gnomad	rs1064793853
Varsome	rs1064793853
LitVar	rs1064793853
Map	rs1064793853
PheGenI	rs1064793853
Biobank	rs1064793853
1000 genomes	rs1064793853
hgdp	rs1064793853
ensembl	rs1064793853
geneview	rs1064793853
scholar	rs1064793853
google	rs1064793853
pharmgkb	rs1064793853
gwascentral	rs1064793853
openSNP	rs1064793853
23andMe	rs1064793853
SNPshot	rs1064793853
SNPdbe	rs1064793853
MSV3d	rs1064793853
GWAS Ctlg	rs1064793853

Max Magnitude

0

ClinVar
Risk	rs1064793853(-;-)
Alt	rs1064793853(-;-)
Reference	Rs1064793853(AT;AT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	NTHL1 TSC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.2098747_2098748delTA
CLNSRC
CLNACC	RCV000481383.1,