rs863223828

Orientation

plus

Stabilized

plus

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

Make rs863223828(A;C)

Make rs863223828(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

99149259

Gene

TGFBR1

is a	snp
is	mentioned by
dbSNP	rs863223828
dbSNP (classic)	rs863223828
ClinGen	rs863223828
ebi	rs863223828
HLI	rs863223828
Exac	rs863223828
Gnomad	rs863223828
Varsome	rs863223828
LitVar	rs863223828
Map	rs863223828
PheGenI	rs863223828
Biobank	rs863223828
1000 genomes	rs863223828
hgdp	rs863223828
ensembl	rs863223828
geneview	rs863223828
scholar	rs863223828
google	rs863223828
pharmgkb	rs863223828
gwascentral	rs863223828
openSNP	rs863223828
23andMe	rs863223828
SNPshot	rs863223828
SNPdbe	rs863223828
MSV3d	rs863223828
GWAS Ctlg	rs863223828

Max Magnitude

0

ClinVar
Risk	rs863223828(C;C)
Alt	rs863223828(C;C)
Reference	Rs863223828(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFBR1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.101911541A>C
CLNSRC
CLNACC	RCV000199055.1,