rs397508580

Orientation

plus

Stabilized

plus

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

Make rs397508580(-;-)

Make rs397508580(-;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117627593

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508580
dbSNP (classic)	rs397508580
ClinGen	rs397508580
ebi	rs397508580
HLI	rs397508580
Exac	rs397508580
Gnomad	rs397508580
Varsome	rs397508580
LitVar	rs397508580
Map	rs397508580
PheGenI	rs397508580
Biobank	rs397508580
1000 genomes	rs397508580
hgdp	rs397508580
ensembl	rs397508580
geneview	rs397508580
scholar	rs397508580
google	rs397508580
pharmgkb	rs397508580
gwascentral	rs397508580
openSNP	rs397508580
23andMe	rs397508580
SNPshot	rs397508580
SNPdbe	rs397508580
MSV3d	rs397508580
GWAS Ctlg	rs397508580

Max Magnitude

0

ClinVar
Risk	rs397508580(-;-)
Alt	rs397508580(-;-)
Reference	Rs397508580(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117267647delA
CLNSRC	ClinVar
CLNACC	RCV000046924.2,