rs397508733

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	3	carrier of a cystic fibrosis allele

Make rs397508733(A;A)

Make rs397508733(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

117531114

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508733
dbSNP (classic)	rs397508733
ClinGen	rs397508733
ebi	rs397508733
HLI	rs397508733
Exac	rs397508733
Gnomad	rs397508733
Varsome	rs397508733
LitVar	rs397508733
Map	rs397508733
PheGenI	rs397508733
Biobank	rs397508733
1000 genomes	rs397508733
hgdp	rs397508733
ensembl	rs397508733
geneview	rs397508733
scholar	rs397508733
google	rs397508733
pharmgkb	rs397508733
gwascentral	rs397508733
openSNP	rs397508733
23andMe	rs397508733
SNPshot	rs397508733
SNPdbe	rs397508733
MSV3d	rs397508733
GWAS Ctlg	rs397508733

Max Magnitude

3

ClinVar
Risk	rs397508733(A;A)
Alt	rs397508733(A;A)
Reference	Rs397508733(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117171168G>A
CLNSRC
CLNACC	RCV000047163.2,