rs863223811

Orientation

plus

Stabilized

plus

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

Make rs863223811(C;C)

Make rs863223811(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

99137980

Gene

TGFBR1

is a	snp
is	mentioned by
dbSNP	rs863223811
dbSNP (classic)	rs863223811
ClinGen	rs863223811
ebi	rs863223811
HLI	rs863223811
Exac	rs863223811
Gnomad	rs863223811
Varsome	rs863223811
LitVar	rs863223811
Map	rs863223811
PheGenI	rs863223811
Biobank	rs863223811
1000 genomes	rs863223811
hgdp	rs863223811
ensembl	rs863223811
geneview	rs863223811
scholar	rs863223811
google	rs863223811
pharmgkb	rs863223811
gwascentral	rs863223811
openSNP	rs863223811
23andMe	rs863223811
SNPshot	rs863223811
SNPdbe	rs863223811
MSV3d	rs863223811
GWAS Ctlg	rs863223811

Max Magnitude

0

ClinVar
Risk	rs863223811(C;C)
Alt	rs863223811(C;C)
Reference	Rs863223811(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFBR1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.101900262G>C
CLNSRC
CLNACC	RCV000200533.1,