rs397508582

Orientation

plus

Stabilized

plus

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

Make rs397508582(C;T)

Make rs397508582(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117627609

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508582
dbSNP (classic)	rs397508582
ClinGen	rs397508582
ebi	rs397508582
HLI	rs397508582
Exac	rs397508582
Gnomad	rs397508582
Varsome	rs397508582
LitVar	rs397508582
Map	rs397508582
PheGenI	rs397508582
Biobank	rs397508582
1000 genomes	rs397508582
hgdp	rs397508582
ensembl	rs397508582
geneview	rs397508582
scholar	rs397508582
google	rs397508582
pharmgkb	rs397508582
gwascentral	rs397508582
openSNP	rs397508582
23andMe	rs397508582
SNPshot	rs397508582
SNPdbe	rs397508582
MSV3d	rs397508582
GWAS Ctlg	rs397508582

Max Magnitude

0

ClinVar
Risk	rs397508582(T;T)
Alt	rs397508582(T;T)
Reference	Rs397508582(C;C)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117267663C>T
CLNSRC	ClinVar
CLNACC	RCV000046926.2,