rs397508608

Orientation

plus

Stabilized

plus

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

Make rs397508608(-;G)

Make rs397508608(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117642494

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508608
dbSNP (classic)	rs397508608
ClinGen	rs397508608
ebi	rs397508608
HLI	rs397508608
Exac	rs397508608
Gnomad	rs397508608
Varsome	rs397508608
LitVar	rs397508608
Map	rs397508608
PheGenI	rs397508608
Biobank	rs397508608
1000 genomes	rs397508608
hgdp	rs397508608
ensembl	rs397508608
geneview	rs397508608
scholar	rs397508608
google	rs397508608
pharmgkb	rs397508608
gwascentral	rs397508608
openSNP	rs397508608
23andMe	rs397508608
SNPshot	rs397508608
SNPdbe	rs397508608
MSV3d	rs397508608
GWAS Ctlg	rs397508608

Max Magnitude

0

ClinVar
Risk	rs397508608(G;G)
Alt	rs397508608(G;G)
Reference	Rs397508608(-;-)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117282548dupG
CLNSRC	ClinVar
CLNACC	RCV000046982.2,