rs397508365

Orientation

plus

Stabilized

plus

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

Make rs397508365(C;G)

Make rs397508365(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117592494

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508365
dbSNP (classic)	rs397508365
ClinGen	rs397508365
ebi	rs397508365
HLI	rs397508365
Exac	rs397508365
Gnomad	rs397508365
Varsome	rs397508365
LitVar	rs397508365
Map	rs397508365
PheGenI	rs397508365
Biobank	rs397508365
1000 genomes	rs397508365
hgdp	rs397508365
ensembl	rs397508365
geneview	rs397508365
scholar	rs397508365
google	rs397508365
pharmgkb	rs397508365
gwascentral	rs397508365
openSNP	rs397508365
23andMe	rs397508365
SNPshot	rs397508365
SNPdbe	rs397508365
MSV3d	rs397508365
GWAS Ctlg	rs397508365

Max Magnitude

0

ClinVar
Risk	rs397508365(G;G)
Alt	rs397508365(G;G)
Reference	Rs397508365(C;C)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117232548C>G
CLNSRC	ClinVar
CLNACC	RCV000046576.2,