rs397508273

Orientation

plus

Stabilized

plus

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

Make rs397508273(A;A)

Make rs397508273(A;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117590376

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508273
dbSNP (classic)	rs397508273
ClinGen	rs397508273
ebi	rs397508273
HLI	rs397508273
Exac	rs397508273
Gnomad	rs397508273
Varsome	rs397508273
LitVar	rs397508273
Map	rs397508273
PheGenI	rs397508273
Biobank	rs397508273
1000 genomes	rs397508273
hgdp	rs397508273
ensembl	rs397508273
geneview	rs397508273
scholar	rs397508273
google	rs397508273
pharmgkb	rs397508273
gwascentral	rs397508273
openSNP	rs397508273
23andMe	rs397508273
SNPshot	rs397508273
SNPdbe	rs397508273
MSV3d	rs397508273
GWAS Ctlg	rs397508273

Max Magnitude

0

ClinVar
Risk	rs397508273(A;A)
Alt	rs397508273(A;A)
Reference	Rs397508273(T;T)
Significance	Probable-Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117230430T>A
CLNSRC	ClinVar
CLNACC	RCV000046430.2,