rs397508257

Orientation

plus

Stabilized

plus

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

Make rs397508257(-;-)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117587824

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508257
dbSNP (classic)	rs397508257
ClinGen	rs397508257
ebi	rs397508257
HLI	rs397508257
Exac	rs397508257
Gnomad	rs397508257
Varsome	rs397508257
LitVar	rs397508257
Map	rs397508257
PheGenI	rs397508257
Biobank	rs397508257
1000 genomes	rs397508257
hgdp	rs397508257
ensembl	rs397508257
geneview	rs397508257
scholar	rs397508257
google	rs397508257
pharmgkb	rs397508257
gwascentral	rs397508257
openSNP	rs397508257
23andMe	rs397508257
SNPshot	rs397508257
SNPdbe	rs397508257
MSV3d	rs397508257
GWAS Ctlg	rs397508257

Max Magnitude

3

ClinVar
Risk	rs397508257(-;-)
Alt	rs397508257(-;-)
Reference	Rs397508257(C;C)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117227878delC
CLNSRC	ClinVar
CLNACC	RCV000046400.2,