rs397508798

Orientation

plus

Stabilized

plus

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

Make rs397508798(-;-)

Make rs397508798(-;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117504279

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508798
dbSNP (classic)	rs397508798
ClinGen	rs397508798
ebi	rs397508798
HLI	rs397508798
Exac	rs397508798
Gnomad	rs397508798
Varsome	rs397508798
LitVar	rs397508798
Map	rs397508798
PheGenI	rs397508798
Biobank	rs397508798
1000 genomes	rs397508798
hgdp	rs397508798
ensembl	rs397508798
geneview	rs397508798
scholar	rs397508798
google	rs397508798
pharmgkb	rs397508798
gwascentral	rs397508798
openSNP	rs397508798
23andMe	rs397508798
SNPshot	rs397508798
SNPdbe	rs397508798
MSV3d	rs397508798
GWAS Ctlg	rs397508798

Max Magnitude

0

ClinVar
Risk	rs397508798(-;-)
Alt	rs397508798(-;-)
Reference	Rs397508798(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117144333delG
CLNSRC	ClinVar
CLNACC	RCV000047261.2,