rs863223813

Orientation

plus

Stabilized

plus

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

Make rs863223813(A;G)

Make rs863223813(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

99137993

Gene

TGFBR1

is a	snp
is	mentioned by
dbSNP	rs863223813
dbSNP (classic)	rs863223813
ClinGen	rs863223813
ebi	rs863223813
HLI	rs863223813
Exac	rs863223813
Gnomad	rs863223813
Varsome	rs863223813
LitVar	rs863223813
Map	rs863223813
PheGenI	rs863223813
Biobank	rs863223813
1000 genomes	rs863223813
hgdp	rs863223813
ensembl	rs863223813
geneview	rs863223813
scholar	rs863223813
google	rs863223813
pharmgkb	rs863223813
gwascentral	rs863223813
openSNP	rs863223813
23andMe	rs863223813
SNPshot	rs863223813
SNPdbe	rs863223813
MSV3d	rs863223813
GWAS Ctlg	rs863223813

Max Magnitude

0

ClinVar
Risk	rs863223813(G;G)
Alt	rs863223813(G;G)
Reference	Rs863223813(A;A)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	TGFBR1
CLNDBN	not specified
Reversed	0
HGVS	NC_000009.11:g.101900275A>G
CLNSRC
CLNACC	RCV000198846.2,