rs397508637

Orientation

plus

Stabilized

plus

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

Make rs397508637(-;-)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117652876

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508637
dbSNP (classic)	rs397508637
ClinGen	rs397508637
ebi	rs397508637
HLI	rs397508637
Exac	rs397508637
Gnomad	rs397508637
Varsome	rs397508637
LitVar	rs397508637
Map	rs397508637
PheGenI	rs397508637
Biobank	rs397508637
1000 genomes	rs397508637
hgdp	rs397508637
ensembl	rs397508637
geneview	rs397508637
scholar	rs397508637
google	rs397508637
pharmgkb	rs397508637
gwascentral	rs397508637
openSNP	rs397508637
23andMe	rs397508637
SNPshot	rs397508637
SNPdbe	rs397508637
MSV3d	rs397508637
GWAS Ctlg	rs397508637

Max Magnitude

3

ClinVar
Risk	rs397508637(-;-)
Alt	rs397508637(-;-)
Reference	Rs397508637(A;A)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117292930delA
CLNSRC	CFTR2
CLNACC	RCV000047026.3,