rs397508588

Orientation

plus

Stabilized

plus

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

Make rs397508588(A;A)

Make rs397508588(A;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117627670

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508588
dbSNP (classic)	rs397508588
ClinGen	rs397508588
ebi	rs397508588
HLI	rs397508588
Exac	rs397508588
Gnomad	rs397508588
Varsome	rs397508588
LitVar	rs397508588
Map	rs397508588
PheGenI	rs397508588
Biobank	rs397508588
1000 genomes	rs397508588
hgdp	rs397508588
ensembl	rs397508588
geneview	rs397508588
scholar	rs397508588
google	rs397508588
pharmgkb	rs397508588
gwascentral	rs397508588
openSNP	rs397508588
23andMe	rs397508588
SNPshot	rs397508588
SNPdbe	rs397508588
MSV3d	rs397508588
GWAS Ctlg	rs397508588

Max Magnitude

0

ClinVar
Risk	rs397508588(A;A) rs397508588(G;G)
Alt	rs397508588(A;A) rs397508588(G;G)
Reference	Rs397508588(C;C)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117267724C>A; NC_000007.13:g.117267724C>G
CLNSRC	ClinVar
CLNACC	RCV000046937.2, RCV000046938.2,