rs397508559

Orientation

plus

Stabilized

plus

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

Make rs397508559(-;AGTA)

Make rs397508559(AGTA;AGTA)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117614669

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508559
dbSNP (classic)	rs397508559
ClinGen	rs397508559
ebi	rs397508559
HLI	rs397508559
Exac	rs397508559
Gnomad	rs397508559
Varsome	rs397508559
LitVar	rs397508559
Map	rs397508559
PheGenI	rs397508559
Biobank	rs397508559
1000 genomes	rs397508559
hgdp	rs397508559
ensembl	rs397508559
geneview	rs397508559
scholar	rs397508559
google	rs397508559
pharmgkb	rs397508559
gwascentral	rs397508559
openSNP	rs397508559
23andMe	rs397508559
SNPshot	rs397508559
SNPdbe	rs397508559
MSV3d	rs397508559
GWAS Ctlg	rs397508559

Max Magnitude

0

ClinVar
Risk	rs397508559(AGTA;AGTA)
Alt	rs397508559(AGTA;AGTA)
Reference	Rs397508559(-;-)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117254720_117254723dupAGTA
CLNSRC	ClinVar
CLNACC	RCV000046887.2,