rs397508654

Orientation

plus

Stabilized

plus

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

Make rs397508654(-;-)

Make rs397508654(-;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117664700

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508654
dbSNP (classic)	rs397508654
ClinGen	rs397508654
ebi	rs397508654
HLI	rs397508654
Exac	rs397508654
Gnomad	rs397508654
Varsome	rs397508654
LitVar	rs397508654
Map	rs397508654
PheGenI	rs397508654
Biobank	rs397508654
1000 genomes	rs397508654
hgdp	rs397508654
ensembl	rs397508654
geneview	rs397508654
scholar	rs397508654
google	rs397508654
pharmgkb	rs397508654
gwascentral	rs397508654
openSNP	rs397508654
23andMe	rs397508654
SNPshot	rs397508654
SNPdbe	rs397508654
MSV3d	rs397508654
GWAS Ctlg	rs397508654

Max Magnitude

0

ClinVar
Risk	rs397508654(-;-)
Alt	rs397508654(-;-)
Reference	Rs397508654(T;T)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117304754delT
CLNSRC	ClinVar
CLNACC	RCV000047049.2,