rs397508496

Orientation

plus

Stabilized

plus

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

Make rs397508496(C;T)

Make rs397508496(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117610633

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508496
dbSNP (classic)	rs397508496
ClinGen	rs397508496
ebi	rs397508496
HLI	rs397508496
Exac	rs397508496
Gnomad	rs397508496
Varsome	rs397508496
LitVar	rs397508496
Map	rs397508496
PheGenI	rs397508496
Biobank	rs397508496
1000 genomes	rs397508496
hgdp	rs397508496
ensembl	rs397508496
geneview	rs397508496
scholar	rs397508496
google	rs397508496
pharmgkb	rs397508496
gwascentral	rs397508496
openSNP	rs397508496
23andMe	rs397508496
SNPshot	rs397508496
SNPdbe	rs397508496
MSV3d	rs397508496
GWAS Ctlg	rs397508496

Max Magnitude

0

ClinVar
Risk	rs397508496(T;T)
Alt	rs397508496(T;T)
Reference	Rs397508496(C;C)
Significance	Probable-Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117250687C>T
CLNSRC	ClinVar
CLNACC	RCV000046781.2,