rs397508497

Orientation

plus

Stabilized

plus

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

Make rs397508497(-;-)

Make rs397508497(-;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117610636

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508497
dbSNP (classic)	rs397508497
ClinGen	rs397508497
ebi	rs397508497
HLI	rs397508497
Exac	rs397508497
Gnomad	rs397508497
Varsome	rs397508497
LitVar	rs397508497
Map	rs397508497
PheGenI	rs397508497
Biobank	rs397508497
1000 genomes	rs397508497
hgdp	rs397508497
ensembl	rs397508497
geneview	rs397508497
scholar	rs397508497
google	rs397508497
pharmgkb	rs397508497
gwascentral	rs397508497
openSNP	rs397508497
23andMe	rs397508497
SNPshot	rs397508497
SNPdbe	rs397508497
MSV3d	rs397508497
GWAS Ctlg	rs397508497

Max Magnitude

0

ClinVar
Risk	rs397508497(-;-)
Alt	rs397508497(-;-)
Reference	Rs397508497(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117250690delA
CLNSRC	ClinVar
CLNACC	RCV000046782.2,