rs397508485

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;C)	3	carrier of a cystic fibrosis allele

Make rs397508485(C;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117610569

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508485
dbSNP (classic)	rs397508485
ClinGen	rs397508485
ebi	rs397508485
HLI	rs397508485
Exac	rs397508485
Gnomad	rs397508485
Varsome	rs397508485
LitVar	rs397508485
Map	rs397508485
PheGenI	rs397508485
Biobank	rs397508485
1000 genomes	rs397508485
hgdp	rs397508485
ensembl	rs397508485
geneview	rs397508485
scholar	rs397508485
google	rs397508485
pharmgkb	rs397508485
gwascentral	rs397508485
openSNP	rs397508485
23andMe	rs397508485
SNPshot	rs397508485
SNPdbe	rs397508485
MSV3d	rs397508485
GWAS Ctlg	rs397508485

Max Magnitude

3

ClinVar
Risk	rs397508485(C;C)
Alt	rs397508485(C;C)
Reference	Rs397508485(-;-)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117250623dupC
CLNSRC	ClinVar
CLNACC	RCV000046764.2,