rs397508661

Orientation

plus

Stabilized

plus

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

Make rs397508661(-;GGGG)

Make rs397508661(GGGG;GGGG)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117664752

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508661
dbSNP (classic)	rs397508661
ClinGen	rs397508661
ebi	rs397508661
HLI	rs397508661
Exac	rs397508661
Gnomad	rs397508661
Varsome	rs397508661
LitVar	rs397508661
Map	rs397508661
PheGenI	rs397508661
Biobank	rs397508661
1000 genomes	rs397508661
hgdp	rs397508661
ensembl	rs397508661
geneview	rs397508661
scholar	rs397508661
google	rs397508661
pharmgkb	rs397508661
gwascentral	rs397508661
openSNP	rs397508661
23andMe	rs397508661
SNPshot	rs397508661
SNPdbe	rs397508661
MSV3d	rs397508661
GWAS Ctlg	rs397508661

Max Magnitude

0

ClinVar
Risk	rs397508661(GGGG;GGGG)
Alt	rs397508661(GGGG;GGGG)
Reference	Rs397508661(-;-)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117304803_117304806dupGGGG
CLNSRC	ClinVar
CLNACC	RCV000047058.2,