rs397508561

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	3	carrier of a cystic fibrosis allele
(G;G)	0	common in clinvar

Make rs397508561(A;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117614680

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508561
dbSNP (classic)	rs397508561
ClinGen	rs397508561
ebi	rs397508561
HLI	rs397508561
Exac	rs397508561
Gnomad	rs397508561
Varsome	rs397508561
LitVar	rs397508561
Map	rs397508561
PheGenI	rs397508561
Biobank	rs397508561
1000 genomes	rs397508561
hgdp	rs397508561
ensembl	rs397508561
geneview	rs397508561
scholar	rs397508561
google	rs397508561
pharmgkb	rs397508561
gwascentral	rs397508561
openSNP	rs397508561
23andMe	rs397508561
SNPshot	rs397508561
SNPdbe	rs397508561
MSV3d	rs397508561
GWAS Ctlg	rs397508561

Max Magnitude

3

ClinVar
Risk	rs397508561(A;A)
Alt	rs397508561(A;A)
Reference	Rs397508561(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117254734G>A
CLNSRC	ClinVar
CLNACC	RCV000046889.2,