rs397508396

Orientation

plus

Stabilized

plus

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

Make rs397508396(-;-)

Make rs397508396(-;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117595001

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508396
dbSNP (classic)	rs397508396
ClinGen	rs397508396
ebi	rs397508396
HLI	rs397508396
Exac	rs397508396
Gnomad	rs397508396
Varsome	rs397508396
LitVar	rs397508396
Map	rs397508396
PheGenI	rs397508396
Biobank	rs397508396
1000 genomes	rs397508396
hgdp	rs397508396
ensembl	rs397508396
geneview	rs397508396
scholar	rs397508396
google	rs397508396
pharmgkb	rs397508396
gwascentral	rs397508396
openSNP	rs397508396
23andMe	rs397508396
SNPshot	rs397508396
SNPdbe	rs397508396
MSV3d	rs397508396
GWAS Ctlg	rs397508396

Max Magnitude

0

ClinVar
Risk	rs397508396(-;-)
Alt	rs397508396(-;-)
Reference	Rs397508396(T;T)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117235055delT
CLNSRC	ClinVar
CLNACC	RCV000046620.2,