rs397508767

Orientation

plus

Stabilized

plus

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

Make rs397508767(-;-)

Make rs397508767(-;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117535269

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508767
dbSNP (classic)	rs397508767
ClinGen	rs397508767
ebi	rs397508767
HLI	rs397508767
Exac	rs397508767
Gnomad	rs397508767
Varsome	rs397508767
LitVar	rs397508767
Map	rs397508767
PheGenI	rs397508767
Biobank	rs397508767
1000 genomes	rs397508767
hgdp	rs397508767
ensembl	rs397508767
geneview	rs397508767
scholar	rs397508767
google	rs397508767
pharmgkb	rs397508767
gwascentral	rs397508767
openSNP	rs397508767
23andMe	rs397508767
SNPshot	rs397508767
SNPdbe	rs397508767
MSV3d	rs397508767
GWAS Ctlg	rs397508767

Max Magnitude

0

ClinVar
Risk	rs397508767(-;-)
Alt	rs397508767(-;-)
Reference	Rs397508767(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117175323delG
CLNSRC	ClinVar
CLNACC	RCV000047216.2,