rs1057520098

Orientation

plus

Stabilized

plus

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

Make rs1057520098(G;T)

Make rs1057520098(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

22

Position

30617488

Gene

TCN2

is a	snp
is	mentioned by
dbSNP	rs1057520098
dbSNP (classic)	rs1057520098
ClinGen	rs1057520098
ebi	rs1057520098
HLI	rs1057520098
Exac	rs1057520098
Gnomad	rs1057520098
Varsome	rs1057520098
LitVar	rs1057520098
Map	rs1057520098
PheGenI	rs1057520098
Biobank	rs1057520098
1000 genomes	rs1057520098
hgdp	rs1057520098
ensembl	rs1057520098
geneview	rs1057520098
scholar	rs1057520098
google	rs1057520098
pharmgkb	rs1057520098
gwascentral	rs1057520098
openSNP	rs1057520098
23andMe	rs1057520098
SNPshot	rs1057520098
SNPdbe	rs1057520098
MSV3d	rs1057520098
GWAS Ctlg	rs1057520098

Max Magnitude

0

ClinVar
Risk	rs1057520098(T;T)
Alt	rs1057520098(T;T)
Reference	Rs1057520098(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TCN2
CLNDBN	not provided
Reversed	0
HGVS	NC_000022.10:g.31013475G>T
CLNSRC
CLNACC	RCV000434122.1,