rs397508372

Orientation

plus

Stabilized

plus

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

Make rs397508372(-;C)

Make rs397508372(C;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117592557

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508372
dbSNP (classic)	rs397508372
ClinGen	rs397508372
ebi	rs397508372
HLI	rs397508372
Exac	rs397508372
Gnomad	rs397508372
Varsome	rs397508372
LitVar	rs397508372
Map	rs397508372
PheGenI	rs397508372
Biobank	rs397508372
1000 genomes	rs397508372
hgdp	rs397508372
ensembl	rs397508372
geneview	rs397508372
scholar	rs397508372
google	rs397508372
pharmgkb	rs397508372
gwascentral	rs397508372
openSNP	rs397508372
23andMe	rs397508372
SNPshot	rs397508372
SNPdbe	rs397508372
MSV3d	rs397508372
GWAS Ctlg	rs397508372

Max Magnitude

0

ClinVar
Risk	rs397508372(C;C)
Alt	rs397508372(C;C)
Reference	Rs397508372(-;-)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117232612dupC
CLNSRC	ClinVar
CLNACC	RCV000046587.2,