rs397508614

Orientation

plus

Stabilized

plus

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

Make rs397508614(-;-)

Make rs397508614(-;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117642549

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508614
dbSNP (classic)	rs397508614
ClinGen	rs397508614
ebi	rs397508614
HLI	rs397508614
Exac	rs397508614
Gnomad	rs397508614
Varsome	rs397508614
LitVar	rs397508614
Map	rs397508614
PheGenI	rs397508614
Biobank	rs397508614
1000 genomes	rs397508614
hgdp	rs397508614
ensembl	rs397508614
geneview	rs397508614
scholar	rs397508614
google	rs397508614
pharmgkb	rs397508614
gwascentral	rs397508614
openSNP	rs397508614
23andMe	rs397508614
SNPshot	rs397508614
SNPdbe	rs397508614
MSV3d	rs397508614
GWAS Ctlg	rs397508614

Max Magnitude

0

ClinVar
Risk	rs397508614(-;-)
Alt	rs397508614(-;-)
Reference	Rs397508614(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117282603delA
CLNSRC	ClinVar
CLNACC	RCV000046990.2,