rs397508278

Orientation

plus

Stabilized

plus

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

Make rs397508278(A;A)

Make rs397508278(A;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117590380

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508278
dbSNP (classic)	rs397508278
ClinGen	rs397508278
ebi	rs397508278
HLI	rs397508278
Exac	rs397508278
Gnomad	rs397508278
Varsome	rs397508278
LitVar	rs397508278
Map	rs397508278
PheGenI	rs397508278
Biobank	rs397508278
1000 genomes	rs397508278
hgdp	rs397508278
ensembl	rs397508278
geneview	rs397508278
scholar	rs397508278
google	rs397508278
pharmgkb	rs397508278
gwascentral	rs397508278
openSNP	rs397508278
23andMe	rs397508278
SNPshot	rs397508278
SNPdbe	rs397508278
MSV3d	rs397508278
GWAS Ctlg	rs397508278

Max Magnitude

0

ClinVar
Risk	rs397508278(A;A) rs397508278(C;C)
Alt	rs397508278(A;A) rs397508278(C;C)
Reference	Rs397508278(T;T)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117230434T>A
CLNSRC	ClinVar
CLNACC	RCV000046436.2,