rs1256196

Orientation

plus

Stabilized

plus

Make rs1256196(A;A)

Make rs1256196(A;T)

Make rs1256196(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

122641075

is a	snp
is	mentioned by
dbSNP	rs1256196
dbSNP (classic)	rs1256196
ClinGen	rs1256196
ebi	rs1256196
HLI	rs1256196
Exac	rs1256196
Gnomad	rs1256196
Varsome	rs1256196
LitVar	rs1256196
Map	rs1256196
PheGenI	rs1256196
Biobank	rs1256196
1000 genomes	rs1256196
hgdp	rs1256196
ensembl	rs1256196
geneview	rs1256196
scholar	rs1256196
google	rs1256196
pharmgkb	rs1256196
gwascentral	rs1256196
openSNP	rs1256196
23andMe	rs1256196
SNPshot	rs1256196
SNPdbe	rs1256196
MSV3d	rs1256196
GWAS Ctlg	rs1256196

GMAF

0.3035

Max Magnitude

0

?	(A;A) (A;T) (T;T)	28

OMIM	121009
Desc	CONNECTIVE TISSUE GROWTH FACTOR; CTGF
Variant
Related	also

OMIM	604201
Desc
Variant
Related	also

[PMID 19822645] Variants of CTGF are associated with hepatic fibrosis in Chinese, Sudanese, and Brazilians infected with schistosomes.