rs397508462

Orientation

plus

Stabilized

plus

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

Make rs397508462(A;C)

Make rs397508462(C;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117606701

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508462
dbSNP (classic)	rs397508462
ClinGen	rs397508462
ebi	rs397508462
HLI	rs397508462
Exac	rs397508462
Gnomad	rs397508462
Varsome	rs397508462
LitVar	rs397508462
Map	rs397508462
PheGenI	rs397508462
Biobank	rs397508462
1000 genomes	rs397508462
hgdp	rs397508462
ensembl	rs397508462
geneview	rs397508462
scholar	rs397508462
google	rs397508462
pharmgkb	rs397508462
gwascentral	rs397508462
openSNP	rs397508462
23andMe	rs397508462
SNPshot	rs397508462
SNPdbe	rs397508462
MSV3d	rs397508462
GWAS Ctlg	rs397508462

Max Magnitude

3

ClinVar
Risk	rs397508462(C;C) rs397508462(T;T)
Alt	rs397508462(C;C) rs397508462(T;T)
Reference	Rs397508462(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117246755A>C; NC_000007.13:g.117246755A>T
CLNSRC	ClinVar
CLNACC	RCV000046727.2, RCV000046728.2,