rs397508663

Orientation

plus

Stabilized

plus

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

Make rs397508663(-;A)

Make rs397508663(A;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117664763

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508663
dbSNP (classic)	rs397508663
ClinGen	rs397508663
ebi	rs397508663
HLI	rs397508663
Exac	rs397508663
Gnomad	rs397508663
Varsome	rs397508663
LitVar	rs397508663
Map	rs397508663
PheGenI	rs397508663
Biobank	rs397508663
1000 genomes	rs397508663
hgdp	rs397508663
ensembl	rs397508663
geneview	rs397508663
scholar	rs397508663
google	rs397508663
pharmgkb	rs397508663
gwascentral	rs397508663
openSNP	rs397508663
23andMe	rs397508663
SNPshot	rs397508663
SNPdbe	rs397508663
MSV3d	rs397508663
GWAS Ctlg	rs397508663

Max Magnitude

0

ClinVar
Risk	rs397508663(A;A)
Alt	rs397508663(A;A)
Reference	Rs397508663(-;-)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117304817dupA
CLNSRC	ClinVar
CLNACC	RCV000047060.2,