rs397508530

Orientation

plus

Stabilized

plus

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

Make rs397508530(-;-)

Make rs397508530(-;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117530953

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508530
dbSNP (classic)	rs397508530
ClinGen	rs397508530
ebi	rs397508530
HLI	rs397508530
Exac	rs397508530
Gnomad	rs397508530
Varsome	rs397508530
LitVar	rs397508530
Map	rs397508530
PheGenI	rs397508530
Biobank	rs397508530
1000 genomes	rs397508530
hgdp	rs397508530
ensembl	rs397508530
geneview	rs397508530
scholar	rs397508530
google	rs397508530
pharmgkb	rs397508530
gwascentral	rs397508530
openSNP	rs397508530
23andMe	rs397508530
SNPshot	rs397508530
SNPdbe	rs397508530
MSV3d	rs397508530
GWAS Ctlg	rs397508530

Max Magnitude

0

ClinVar
Risk	rs397508530(-;-)
Alt	rs397508530(-;-)
Reference	Rs397508530(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117171007delG
CLNSRC	ClinVar
CLNACC	RCV000046853.2,