rs397508626

Orientation

plus

Stabilized

plus

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

Make rs397508626(-;-)

Make rs397508626(-;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117652844

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508626
dbSNP (classic)	rs397508626
ClinGen	rs397508626
ebi	rs397508626
HLI	rs397508626
Exac	rs397508626
Gnomad	rs397508626
Varsome	rs397508626
LitVar	rs397508626
Map	rs397508626
PheGenI	rs397508626
Biobank	rs397508626
1000 genomes	rs397508626
hgdp	rs397508626
ensembl	rs397508626
geneview	rs397508626
scholar	rs397508626
google	rs397508626
pharmgkb	rs397508626
gwascentral	rs397508626
openSNP	rs397508626
23andMe	rs397508626
SNPshot	rs397508626
SNPdbe	rs397508626
MSV3d	rs397508626
GWAS Ctlg	rs397508626

Max Magnitude

0

ClinVar
Risk	rs397508626(-;-)
Alt	rs397508626(-;-)
Reference	Rs397508626(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117292898delA
CLNSRC	ClinVar
CLNACC	RCV000047012.2,