rs397508234

Orientation

plus

Stabilized

plus

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

Make rs397508234(A;A)

Make rs397508234(A;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117587730

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508234
dbSNP (classic)	rs397508234
ClinGen	rs397508234
ebi	rs397508234
HLI	rs397508234
Exac	rs397508234
Gnomad	rs397508234
Varsome	rs397508234
LitVar	rs397508234
Map	rs397508234
PheGenI	rs397508234
Biobank	rs397508234
1000 genomes	rs397508234
hgdp	rs397508234
ensembl	rs397508234
geneview	rs397508234
scholar	rs397508234
google	rs397508234
pharmgkb	rs397508234
gwascentral	rs397508234
openSNP	rs397508234
23andMe	rs397508234
SNPshot	rs397508234
SNPdbe	rs397508234
MSV3d	rs397508234
GWAS Ctlg	rs397508234

Max Magnitude

0

ClinVar
Risk	rs397508234(A;A)
Alt	rs397508234(A;A)
Reference	Rs397508234(T;T)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117227784T>A
CLNSRC	ClinVar
CLNACC	RCV000046354.2,