rs397508389

Orientation

plus

Stabilized

plus

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

Make rs397508389(-;T)

Make rs397508389(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117594941

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508389
dbSNP (classic)	rs397508389
ClinGen	rs397508389
ebi	rs397508389
HLI	rs397508389
Exac	rs397508389
Gnomad	rs397508389
Varsome	rs397508389
LitVar	rs397508389
Map	rs397508389
PheGenI	rs397508389
Biobank	rs397508389
1000 genomes	rs397508389
hgdp	rs397508389
ensembl	rs397508389
geneview	rs397508389
scholar	rs397508389
google	rs397508389
pharmgkb	rs397508389
gwascentral	rs397508389
openSNP	rs397508389
23andMe	rs397508389
SNPshot	rs397508389
SNPdbe	rs397508389
MSV3d	rs397508389
GWAS Ctlg	rs397508389

Max Magnitude

0

ClinVar
Risk	rs397508389(T;T)
Alt	rs397508389(T;T)
Reference	Rs397508389(-;-)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117234995dupT
CLNSRC	ClinVar
CLNACC	RCV000046608.2,