rs397508388

Orientation

plus

Stabilized

plus

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

Make rs397508388(A;A)

Make rs397508388(A;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117594935

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508388
dbSNP (classic)	rs397508388
ClinGen	rs397508388
ebi	rs397508388
HLI	rs397508388
Exac	rs397508388
Gnomad	rs397508388
Varsome	rs397508388
LitVar	rs397508388
Map	rs397508388
PheGenI	rs397508388
Biobank	rs397508388
1000 genomes	rs397508388
hgdp	rs397508388
ensembl	rs397508388
geneview	rs397508388
scholar	rs397508388
google	rs397508388
pharmgkb	rs397508388
gwascentral	rs397508388
openSNP	rs397508388
23andMe	rs397508388
SNPshot	rs397508388
SNPdbe	rs397508388
MSV3d	rs397508388
GWAS Ctlg	rs397508388

Max Magnitude

0

ClinVar
Risk	rs397508388(A;A)
Alt	rs397508388(A;A)
Reference	Rs397508388(C;C)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117234989C>A
CLNSRC	ClinVar
CLNACC	RCV000046607.2,