rs397508569

Orientation

plus

Stabilized

plus

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

Make rs397508569(A;G)

Make rs397508569(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117614706

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508569
dbSNP (classic)	rs397508569
ClinGen	rs397508569
ebi	rs397508569
HLI	rs397508569
Exac	rs397508569
Gnomad	rs397508569
Varsome	rs397508569
LitVar	rs397508569
Map	rs397508569
PheGenI	rs397508569
Biobank	rs397508569
1000 genomes	rs397508569
hgdp	rs397508569
ensembl	rs397508569
geneview	rs397508569
scholar	rs397508569
google	rs397508569
pharmgkb	rs397508569
gwascentral	rs397508569
openSNP	rs397508569
23andMe	rs397508569
SNPshot	rs397508569
SNPdbe	rs397508569
MSV3d	rs397508569
GWAS Ctlg	rs397508569

Max Magnitude

0

ClinVar
Risk	rs397508569(G;G) rs397508569(T;T)
Alt	rs397508569(G;G) rs397508569(T;T)
Reference	Rs397508569(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117254760A>G
CLNSRC	ClinVar
CLNACC	RCV000046898.2,