rs397508478

Orientation

plus

Stabilized

plus

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

Make rs397508478(G;T)

Make rs397508478(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117610537

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508478
dbSNP (classic)	rs397508478
ClinGen	rs397508478
ebi	rs397508478
HLI	rs397508478
Exac	rs397508478
Gnomad	rs397508478
Varsome	rs397508478
LitVar	rs397508478
Map	rs397508478
PheGenI	rs397508478
Biobank	rs397508478
1000 genomes	rs397508478
hgdp	rs397508478
ensembl	rs397508478
geneview	rs397508478
scholar	rs397508478
google	rs397508478
pharmgkb	rs397508478
gwascentral	rs397508478
openSNP	rs397508478
23andMe	rs397508478
SNPshot	rs397508478
SNPdbe	rs397508478
MSV3d	rs397508478
GWAS Ctlg	rs397508478

Max Magnitude

0

ClinVar
Risk	rs397508478(T;T)
Alt	rs397508478(T;T)
Reference	Rs397508478(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117250591G>T
CLNSRC	ClinVar
CLNACC	RCV000046753.2,