rs397508151

Orientation

plus

Stabilized

plus

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

Make rs397508151(-;-)

Make rs397508151(-;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117540299

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508151
dbSNP (classic)	rs397508151
ClinGen	rs397508151
ebi	rs397508151
HLI	rs397508151
Exac	rs397508151
Gnomad	rs397508151
Varsome	rs397508151
LitVar	rs397508151
Map	rs397508151
PheGenI	rs397508151
Biobank	rs397508151
1000 genomes	rs397508151
hgdp	rs397508151
ensembl	rs397508151
geneview	rs397508151
scholar	rs397508151
google	rs397508151
pharmgkb	rs397508151
gwascentral	rs397508151
openSNP	rs397508151
23andMe	rs397508151
SNPshot	rs397508151
SNPdbe	rs397508151
MSV3d	rs397508151
GWAS Ctlg	rs397508151

Max Magnitude

0

ClinVar
Risk	rs397508151(-;-)
Alt	rs397508151(-;-)
Reference	Rs397508151(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117180353delG
CLNSRC	ClinVar
CLNACC	RCV000046219.2,