rs397508696

Orientation

plus

Stabilized

plus

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

Make rs397508696(A;A)

Make rs397508696(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117665523

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508696
dbSNP (classic)	rs397508696
ClinGen	rs397508696
ebi	rs397508696
HLI	rs397508696
Exac	rs397508696
Gnomad	rs397508696
Varsome	rs397508696
LitVar	rs397508696
Map	rs397508696
PheGenI	rs397508696
Biobank	rs397508696
1000 genomes	rs397508696
hgdp	rs397508696
ensembl	rs397508696
geneview	rs397508696
scholar	rs397508696
google	rs397508696
pharmgkb	rs397508696
gwascentral	rs397508696
openSNP	rs397508696
23andMe	rs397508696
SNPshot	rs397508696
SNPdbe	rs397508696
MSV3d	rs397508696
GWAS Ctlg	rs397508696

Max Magnitude

0

ClinVar
Risk	rs397508696(A;A) rs397508696(T;T)
Alt	rs397508696(A;A) rs397508696(T;T)
Reference	Rs397508696(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117305577G>A; NC_000007.13:g.117305577G>T
CLNSRC	ClinVar
CLNACC	RCV000047103.2, RCV000047104.2,