rs397508554

Orientation

plus

Stabilized

plus

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

Make rs397508554(A;T)

Make rs397508554(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117530965

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508554
dbSNP (classic)	rs397508554
ClinGen	rs397508554
ebi	rs397508554
HLI	rs397508554
Exac	rs397508554
Gnomad	rs397508554
Varsome	rs397508554
LitVar	rs397508554
Map	rs397508554
PheGenI	rs397508554
Biobank	rs397508554
1000 genomes	rs397508554
hgdp	rs397508554
ensembl	rs397508554
geneview	rs397508554
scholar	rs397508554
google	rs397508554
pharmgkb	rs397508554
gwascentral	rs397508554
openSNP	rs397508554
23andMe	rs397508554
SNPshot	rs397508554
SNPdbe	rs397508554
MSV3d	rs397508554
GWAS Ctlg	rs397508554

Max Magnitude

0

ClinVar
Risk	rs397508554(T;T)
Alt	rs397508554(T;T)
Reference	Rs397508554(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117171019A>T
CLNSRC	ClinVar
CLNACC	RCV000046882.2,