rs397508231

Orientation

plus

Stabilized

plus

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

Make rs397508231(C;C)

Make rs397508231(C;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117559657

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508231
dbSNP (classic)	rs397508231
ClinGen	rs397508231
ebi	rs397508231
HLI	rs397508231
Exac	rs397508231
Gnomad	rs397508231
Varsome	rs397508231
LitVar	rs397508231
Map	rs397508231
PheGenI	rs397508231
Biobank	rs397508231
1000 genomes	rs397508231
hgdp	rs397508231
ensembl	rs397508231
geneview	rs397508231
scholar	rs397508231
google	rs397508231
pharmgkb	rs397508231
gwascentral	rs397508231
openSNP	rs397508231
23andMe	rs397508231
SNPshot	rs397508231
SNPdbe	rs397508231
MSV3d	rs397508231
GWAS Ctlg	rs397508231

Max Magnitude

0

ClinVar
Risk	rs397508231(C;C)
Alt	rs397508231(C;C)
Reference	Rs397508231(T;T)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117199711T>C
CLNSRC	ClinVar
CLNACC	RCV000046348.2,