rs397508583

Orientation

plus

Stabilized

plus

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

Make rs397508583(-;-)

Make rs397508583(-;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117530982

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508583
dbSNP (classic)	rs397508583
ClinGen	rs397508583
ebi	rs397508583
HLI	rs397508583
Exac	rs397508583
Gnomad	rs397508583
Varsome	rs397508583
LitVar	rs397508583
Map	rs397508583
PheGenI	rs397508583
Biobank	rs397508583
1000 genomes	rs397508583
hgdp	rs397508583
ensembl	rs397508583
geneview	rs397508583
scholar	rs397508583
google	rs397508583
pharmgkb	rs397508583
gwascentral	rs397508583
openSNP	rs397508583
23andMe	rs397508583
SNPshot	rs397508583
SNPdbe	rs397508583
MSV3d	rs397508583
GWAS Ctlg	rs397508583

Max Magnitude

0

ClinVar
Risk	rs397508583(-;-)
Alt	rs397508583(-;-)
Reference	Rs397508583(C;C)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117171036delC
CLNSRC	ClinVar
CLNACC	RCV000046927.2,