rs397508552

Orientation

plus

Stabilized

plus

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

Make rs397508552(AC;GTA)

Make rs397508552(GTA;GTA)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117614645

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508552
dbSNP (classic)	rs397508552
ClinGen	rs397508552
ebi	rs397508552
HLI	rs397508552
Exac	rs397508552
Gnomad	rs397508552
Varsome	rs397508552
LitVar	rs397508552
Map	rs397508552
PheGenI	rs397508552
Biobank	rs397508552
1000 genomes	rs397508552
hgdp	rs397508552
ensembl	rs397508552
geneview	rs397508552
scholar	rs397508552
google	rs397508552
pharmgkb	rs397508552
gwascentral	rs397508552
openSNP	rs397508552
23andMe	rs397508552
SNPshot	rs397508552
SNPdbe	rs397508552
MSV3d	rs397508552
GWAS Ctlg	rs397508552

Max Magnitude

0

ClinVar
Risk	rs397508552(GTA;GTA)
Alt	rs397508552(GTA;GTA)
Reference	Rs397508552(AC;AC)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117254699_117254700delACinsGTA
CLNSRC	ClinVar
CLNACC	RCV000046880.2,