rs397508443

Orientation

plus

Stabilized

plus

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

Make rs397508443(A;T)

Make rs397508443(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117603710

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508443
dbSNP (classic)	rs397508443
ClinGen	rs397508443
ebi	rs397508443
HLI	rs397508443
Exac	rs397508443
Gnomad	rs397508443
Varsome	rs397508443
LitVar	rs397508443
Map	rs397508443
PheGenI	rs397508443
Biobank	rs397508443
1000 genomes	rs397508443
hgdp	rs397508443
ensembl	rs397508443
geneview	rs397508443
scholar	rs397508443
google	rs397508443
pharmgkb	rs397508443
gwascentral	rs397508443
openSNP	rs397508443
23andMe	rs397508443
SNPshot	rs397508443
SNPdbe	rs397508443
MSV3d	rs397508443
GWAS Ctlg	rs397508443

Max Magnitude

0

ClinVar
Risk	rs397508443(T;T)
Alt	rs397508443(T;T)
Reference	Rs397508443(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117243764A>T
CLNSRC	ClinVar
CLNACC	RCV000046698.2,