rs397508334

Orientation

plus

Stabilized

plus

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

Make rs397508334(-;C)

Make rs397508334(C;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117592211

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508334
dbSNP (classic)	rs397508334
ClinGen	rs397508334
ebi	rs397508334
HLI	rs397508334
Exac	rs397508334
Gnomad	rs397508334
Varsome	rs397508334
LitVar	rs397508334
Map	rs397508334
PheGenI	rs397508334
Biobank	rs397508334
1000 genomes	rs397508334
hgdp	rs397508334
ensembl	rs397508334
geneview	rs397508334
scholar	rs397508334
google	rs397508334
pharmgkb	rs397508334
gwascentral	rs397508334
openSNP	rs397508334
23andMe	rs397508334
SNPshot	rs397508334
SNPdbe	rs397508334
MSV3d	rs397508334
GWAS Ctlg	rs397508334

Max Magnitude

0

ClinVar
Risk	rs397508334(C;C)
Alt	rs397508334(C;C)
Reference	Rs397508334(-;-)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117232266dupC
CLNSRC	ClinVar
CLNACC	RCV000046526.2,