rs397508529

Orientation

plus

Stabilized

plus

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

Make rs397508529(-;-)

Make rs397508529(-;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117611728

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508529
dbSNP (classic)	rs397508529
ClinGen	rs397508529
ebi	rs397508529
HLI	rs397508529
Exac	rs397508529
Gnomad	rs397508529
Varsome	rs397508529
LitVar	rs397508529
Map	rs397508529
PheGenI	rs397508529
Biobank	rs397508529
1000 genomes	rs397508529
hgdp	rs397508529
ensembl	rs397508529
geneview	rs397508529
scholar	rs397508529
google	rs397508529
pharmgkb	rs397508529
gwascentral	rs397508529
openSNP	rs397508529
23andMe	rs397508529
SNPshot	rs397508529
SNPdbe	rs397508529
MSV3d	rs397508529
GWAS Ctlg	rs397508529

Max Magnitude

0

ClinVar
Risk	rs397508529(-;-)
Alt	rs397508529(-;-)
Reference	Rs397508529(T;T)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117251782delT
CLNSRC	ClinVar
CLNACC	RCV000046850.2,