rs397508413

Orientation

plus

Stabilized

plus

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

Make rs397508413(A;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117602851

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508413
dbSNP (classic)	rs397508413
ClinGen	rs397508413
ebi	rs397508413
HLI	rs397508413
Exac	rs397508413
Gnomad	rs397508413
Varsome	rs397508413
LitVar	rs397508413
Map	rs397508413
PheGenI	rs397508413
Biobank	rs397508413
1000 genomes	rs397508413
hgdp	rs397508413
ensembl	rs397508413
geneview	rs397508413
scholar	rs397508413
google	rs397508413
pharmgkb	rs397508413
gwascentral	rs397508413
openSNP	rs397508413
23andMe	rs397508413
SNPshot	rs397508413
SNPdbe	rs397508413
MSV3d	rs397508413
GWAS Ctlg	rs397508413

Max Magnitude

3

ClinVar
Risk	rs397508413(A;A)
Alt	rs397508413(A;A)
Reference	Rs397508413(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117242905G>A
CLNSRC	ClinVar
CLNACC	RCV000046645.2,