rs397508250

Orientation

plus

Stabilized

plus

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

Make rs397508250(A;G)

Make rs397508250(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117509032

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508250
dbSNP (classic)	rs397508250
ClinGen	rs397508250
ebi	rs397508250
HLI	rs397508250
Exac	rs397508250
Gnomad	rs397508250
Varsome	rs397508250
LitVar	rs397508250
Map	rs397508250
PheGenI	rs397508250
Biobank	rs397508250
1000 genomes	rs397508250
hgdp	rs397508250
ensembl	rs397508250
geneview	rs397508250
scholar	rs397508250
google	rs397508250
pharmgkb	rs397508250
gwascentral	rs397508250
openSNP	rs397508250
23andMe	rs397508250
SNPshot	rs397508250
SNPdbe	rs397508250
MSV3d	rs397508250
GWAS Ctlg	rs397508250

Max Magnitude

0

ClinVar
Risk	rs397508250(G;G)
Alt	rs397508250(G;G)
Reference	Rs397508250(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117149086A>G
CLNSRC	ClinVar
CLNACC	RCV000046383.2,