rs397508380

Orientation

plus

Stabilized

plus

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

Make rs397508380(-;-)

Make rs397508380(-;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117592639

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508380
dbSNP (classic)	rs397508380
ClinGen	rs397508380
ebi	rs397508380
HLI	rs397508380
Exac	rs397508380
Gnomad	rs397508380
Varsome	rs397508380
LitVar	rs397508380
Map	rs397508380
PheGenI	rs397508380
Biobank	rs397508380
1000 genomes	rs397508380
hgdp	rs397508380
ensembl	rs397508380
geneview	rs397508380
scholar	rs397508380
google	rs397508380
pharmgkb	rs397508380
gwascentral	rs397508380
openSNP	rs397508380
23andMe	rs397508380
SNPshot	rs397508380
SNPdbe	rs397508380
MSV3d	rs397508380
GWAS Ctlg	rs397508380

Max Magnitude

0

ClinVar
Risk	rs397508380(-;-)
Alt	rs397508380(-;-)
Reference	Rs397508380(T;T)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117232693delT
CLNSRC	ClinVar
CLNACC	RCV000046597.2,