rs397508613

Orientation

plus

Stabilized

plus

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

Make rs397508613(A;A)

Make rs397508613(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117642542

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508613
dbSNP (classic)	rs397508613
ClinGen	rs397508613
ebi	rs397508613
HLI	rs397508613
Exac	rs397508613
Gnomad	rs397508613
Varsome	rs397508613
LitVar	rs397508613
Map	rs397508613
PheGenI	rs397508613
Biobank	rs397508613
1000 genomes	rs397508613
hgdp	rs397508613
ensembl	rs397508613
geneview	rs397508613
scholar	rs397508613
google	rs397508613
pharmgkb	rs397508613
gwascentral	rs397508613
openSNP	rs397508613
23andMe	rs397508613
SNPshot	rs397508613
SNPdbe	rs397508613
MSV3d	rs397508613
GWAS Ctlg	rs397508613

Max Magnitude

0

ClinVar
Risk	rs397508613(A;A)
Alt	rs397508613(A;A)
Reference	Rs397508613(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117282596G>A
CLNSRC	ClinVar
CLNACC	RCV000046989.2,