rs1057519148

Orientation

minus

Stabilized

minus

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

Make rs1057519148(A;G)

Make rs1057519148(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

115059864

Gene

TNC

is a	snp
is	mentioned by
dbSNP	rs1057519148
dbSNP (classic)	rs1057519148
ClinGen	rs1057519148
ebi	rs1057519148
HLI	rs1057519148
Exac	rs1057519148
Gnomad	rs1057519148
Varsome	rs1057519148
LitVar	rs1057519148
Map	rs1057519148
PheGenI	rs1057519148
Biobank	rs1057519148
1000 genomes	rs1057519148
hgdp	rs1057519148
ensembl	rs1057519148
geneview	rs1057519148
scholar	rs1057519148
google	rs1057519148
pharmgkb	rs1057519148
gwascentral	rs1057519148
openSNP	rs1057519148
23andMe	rs1057519148
SNPshot	rs1057519148
SNPdbe	rs1057519148
MSV3d	rs1057519148
GWAS Ctlg	rs1057519148

Max Magnitude

0

ClinVar
Risk	rs1057519148(G;G)
Alt	rs1057519148(G;G)
Reference	Rs1057519148(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TNC
CLNDBN	not provided
Reversed	1
HGVS	NC_000009.11:g.117822143T>C
CLNSRC
CLNACC	RCV000415906.1,