rs397508252

Orientation

plus

Stabilized

plus

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

Make rs397508252(-;-)

Make rs397508252(-;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117587806

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508252
dbSNP (classic)	rs397508252
ClinGen	rs397508252
ebi	rs397508252
HLI	rs397508252
Exac	rs397508252
Gnomad	rs397508252
Varsome	rs397508252
LitVar	rs397508252
Map	rs397508252
PheGenI	rs397508252
Biobank	rs397508252
1000 genomes	rs397508252
hgdp	rs397508252
ensembl	rs397508252
geneview	rs397508252
scholar	rs397508252
google	rs397508252
pharmgkb	rs397508252
gwascentral	rs397508252
openSNP	rs397508252
23andMe	rs397508252
SNPshot	rs397508252
SNPdbe	rs397508252
MSV3d	rs397508252
GWAS Ctlg	rs397508252

Max Magnitude

0

ClinVar
Risk	rs397508252(-;-)
Alt	rs397508252(-;-)
Reference	Rs397508252(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117227860delG
CLNSRC	ClinVar
CLNACC	RCV000046390.2,