rs778381859

Orientation

plus

Stabilized

plus

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

Make rs778381859(-;-)

Make rs778381859(-;TC)

Reference

GRCh38.p7 38.3/150

Chromosome

22

Position

30614416

Gene

TCN2

is a	snp
is	mentioned by
dbSNP	rs778381859
dbSNP (classic)	rs778381859
ClinGen	rs778381859
ebi	rs778381859
HLI	rs778381859
Exac	rs778381859
Gnomad	rs778381859
Varsome	rs778381859
LitVar	rs778381859
Map	rs778381859
PheGenI	rs778381859
Biobank	rs778381859
1000 genomes	rs778381859
hgdp	rs778381859
ensembl	rs778381859
geneview	rs778381859
scholar	rs778381859
google	rs778381859
pharmgkb	rs778381859
gwascentral	rs778381859
openSNP	rs778381859
23andMe	rs778381859
SNPshot	rs778381859
SNPdbe	rs778381859
MSV3d	rs778381859
GWAS Ctlg	rs778381859

Max Magnitude

0

ClinVar
Risk	rs778381859(-;-)
Alt	rs778381859(-;-)
Reference	Rs778381859(TC;TC)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TCN2
CLNDBN	not provided
Reversed	0
HGVS	NC_000022.10:g.31010403_31010404delTC
CLNSRC
CLNACC	RCV000431820.1,