rs397508657

Orientation

plus

Stabilized

plus

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

Make rs397508657(A;A)

Make rs397508657(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117480097

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508657
dbSNP (classic)	rs397508657
ClinGen	rs397508657
ebi	rs397508657
HLI	rs397508657
Exac	rs397508657
Gnomad	rs397508657
Varsome	rs397508657
LitVar	rs397508657
Map	rs397508657
PheGenI	rs397508657
Biobank	rs397508657
1000 genomes	rs397508657
hgdp	rs397508657
ensembl	rs397508657
geneview	rs397508657
scholar	rs397508657
google	rs397508657
pharmgkb	rs397508657
gwascentral	rs397508657
openSNP	rs397508657
23andMe	rs397508657
SNPshot	rs397508657
SNPdbe	rs397508657
MSV3d	rs397508657
GWAS Ctlg	rs397508657

Max Magnitude

0

ClinVar
Risk	rs397508657(A;A) rs397508657(T;T)
Alt	rs397508657(A;A) rs397508657(T;T)
Reference	Rs397508657(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117120151G>A; NC_000007.13:g.117120151G>T
CLNSRC	ClinVar
CLNACC	RCV000047052.2, RCV000047053.2,