rs796051982

Orientation

plus

Stabilized

plus

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

Make rs796051982(-;GTG)

Make rs796051982(GTG;GTG)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

40411272

Gene

IVD

is a	snp
is	mentioned by
dbSNP	rs796051982
dbSNP (classic)	rs796051982
ClinGen	rs796051982
ebi	rs796051982
HLI	rs796051982
Exac	rs796051982
Gnomad	rs796051982
Varsome	rs796051982
LitVar	rs796051982
Map	rs796051982
PheGenI	rs796051982
Biobank	rs796051982
1000 genomes	rs796051982
hgdp	rs796051982
ensembl	rs796051982
geneview	rs796051982
scholar	rs796051982
google	rs796051982
pharmgkb	rs796051982
gwascentral	rs796051982
openSNP	rs796051982
23andMe	rs796051982
SNPshot	rs796051982
SNPdbe	rs796051982
MSV3d	rs796051982
GWAS Ctlg	rs796051982

Max Magnitude

0

ClinVar
Risk	rs796051982(GTG;GTG)
Alt	rs796051982(GTG;GTG)
Reference	Rs796051982(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	IVD
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.40703469_40703471dupGTG
CLNSRC
CLNACC	RCV000185985.1,