rs199660234

Orientation

plus

Stabilized

plus

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

Make rs199660234(C;G)

Make rs199660234(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

30672249

Gene

TGFBR2

is a	snp
is	mentioned by
dbSNP	rs199660234
dbSNP (classic)	rs199660234
ClinGen	rs199660234
ebi	rs199660234
HLI	rs199660234
Exac	rs199660234
Gnomad	rs199660234
Varsome	rs199660234
LitVar	rs199660234
Map	rs199660234
PheGenI	rs199660234
Biobank	rs199660234
1000 genomes	rs199660234
hgdp	rs199660234
ensembl	rs199660234
geneview	rs199660234
scholar	rs199660234
google	rs199660234
pharmgkb	rs199660234
gwascentral	rs199660234
openSNP	rs199660234
23andMe	rs199660234
SNPshot	rs199660234
SNPdbe	rs199660234
MSV3d	rs199660234
GWAS Ctlg	rs199660234

Max Magnitude

0

ClinVar
Risk	rs199660234(G;G) rs199660234(T;T)
Alt	rs199660234(G;G) rs199660234(T;T)
Reference	Rs199660234(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TGFBR2
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.30713741C>G; NC_000003.11:g.30713741C>T
CLNSRC
CLNACC	RCV000197867.1, RCV000489285.1,