rs397508534

Orientation

plus

Stabilized

plus

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

Make rs397508534(-;-)

Make rs397508534(-;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117611735

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508534
dbSNP (classic)	rs397508534
ClinGen	rs397508534
ebi	rs397508534
HLI	rs397508534
Exac	rs397508534
Gnomad	rs397508534
Varsome	rs397508534
LitVar	rs397508534
Map	rs397508534
PheGenI	rs397508534
Biobank	rs397508534
1000 genomes	rs397508534
hgdp	rs397508534
ensembl	rs397508534
geneview	rs397508534
scholar	rs397508534
google	rs397508534
pharmgkb	rs397508534
gwascentral	rs397508534
openSNP	rs397508534
23andMe	rs397508534
SNPshot	rs397508534
SNPdbe	rs397508534
MSV3d	rs397508534
GWAS Ctlg	rs397508534

Max Magnitude

0

ClinVar
Risk	rs397508534(-;-)
Alt	rs397508534(-;-)
Reference	Rs397508534(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117251789delG
CLNSRC	ClinVar
CLNACC	RCV000046857.2,