rs863223822

Orientation

plus

Stabilized

plus

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

Make rs863223822(A;C)

Make rs863223822(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

99144810

Gene

TGFBR1

is a	snp
is	mentioned by
dbSNP	rs863223822
dbSNP (classic)	rs863223822
ClinGen	rs863223822
ebi	rs863223822
HLI	rs863223822
Exac	rs863223822
Gnomad	rs863223822
Varsome	rs863223822
LitVar	rs863223822
Map	rs863223822
PheGenI	rs863223822
Biobank	rs863223822
1000 genomes	rs863223822
hgdp	rs863223822
ensembl	rs863223822
geneview	rs863223822
scholar	rs863223822
google	rs863223822
pharmgkb	rs863223822
gwascentral	rs863223822
openSNP	rs863223822
23andMe	rs863223822
SNPshot	rs863223822
SNPdbe	rs863223822
MSV3d	rs863223822
GWAS Ctlg	rs863223822

Max Magnitude

0

ClinVar
Risk	rs863223822(C;C)
Alt	rs863223822(C;C)
Reference	Rs863223822(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFBR1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.101907092A>C
CLNSRC
CLNACC	RCV000198106.1,