rs397508505

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;GG)	3	carrier of a cystic fibrosis allele
(GG;GG)	0	common in clinvar

Make rs397508505(-;-)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117610669

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508505
dbSNP (classic)	rs397508505
ClinGen	rs397508505
ebi	rs397508505
HLI	rs397508505
Exac	rs397508505
Gnomad	rs397508505
Varsome	rs397508505
LitVar	rs397508505
Map	rs397508505
PheGenI	rs397508505
Biobank	rs397508505
1000 genomes	rs397508505
hgdp	rs397508505
ensembl	rs397508505
geneview	rs397508505
scholar	rs397508505
google	rs397508505
pharmgkb	rs397508505
gwascentral	rs397508505
openSNP	rs397508505
23andMe	rs397508505
SNPshot	rs397508505
SNPdbe	rs397508505
MSV3d	rs397508505
GWAS Ctlg	rs397508505

Max Magnitude

3

ClinVar
Risk	rs397508505(-;-)
Alt	rs397508505(-;-)
Reference	Rs397508505(GG;GG)
Significance	Probable-Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117250723_117250724delGG
CLNSRC	ClinVar
CLNACC	RCV000046791.3,