rs397508514

Orientation

plus

Stabilized

plus

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

Make rs397508514(A;A)

Make rs397508514(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117611630

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508514
dbSNP (classic)	rs397508514
ClinGen	rs397508514
ebi	rs397508514
HLI	rs397508514
Exac	rs397508514
Gnomad	rs397508514
Varsome	rs397508514
LitVar	rs397508514
Map	rs397508514
PheGenI	rs397508514
Biobank	rs397508514
1000 genomes	rs397508514
hgdp	rs397508514
ensembl	rs397508514
geneview	rs397508514
scholar	rs397508514
google	rs397508514
pharmgkb	rs397508514
gwascentral	rs397508514
openSNP	rs397508514
23andMe	rs397508514
SNPshot	rs397508514
SNPdbe	rs397508514
MSV3d	rs397508514
GWAS Ctlg	rs397508514

Max Magnitude

0

ClinVar
Risk	rs397508514(A;A)
Alt	rs397508514(A;A)
Reference	Rs397508514(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117251684G>A
CLNSRC	ClinVar
CLNACC	RCV000046809.2,