rs397508771

Orientation

plus

Stabilized

plus

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

Make rs397508771(C;T)

Make rs397508771(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117535287

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508771
dbSNP (classic)	rs397508771
ClinGen	rs397508771
ebi	rs397508771
HLI	rs397508771
Exac	rs397508771
Gnomad	rs397508771
Varsome	rs397508771
LitVar	rs397508771
Map	rs397508771
PheGenI	rs397508771
Biobank	rs397508771
1000 genomes	rs397508771
hgdp	rs397508771
ensembl	rs397508771
geneview	rs397508771
scholar	rs397508771
google	rs397508771
pharmgkb	rs397508771
gwascentral	rs397508771
openSNP	rs397508771
23andMe	rs397508771
SNPshot	rs397508771
SNPdbe	rs397508771
MSV3d	rs397508771
GWAS Ctlg	rs397508771

Max Magnitude

0

ClinVar
Risk	rs397508771(T;T)
Alt	rs397508771(T;T)
Reference	Rs397508771(C;C)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117175341C>T
CLNSRC	ClinVar
CLNACC	RCV000047223.2,