rs397508671

Orientation

plus

Stabilized

plus

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

Make rs397508671(-;-)

Make rs397508671(-;CTCC)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117531034

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508671
dbSNP (classic)	rs397508671
ClinGen	rs397508671
ebi	rs397508671
HLI	rs397508671
Exac	rs397508671
Gnomad	rs397508671
Varsome	rs397508671
LitVar	rs397508671
Map	rs397508671
PheGenI	rs397508671
Biobank	rs397508671
1000 genomes	rs397508671
hgdp	rs397508671
ensembl	rs397508671
geneview	rs397508671
scholar	rs397508671
google	rs397508671
pharmgkb	rs397508671
gwascentral	rs397508671
openSNP	rs397508671
23andMe	rs397508671
SNPshot	rs397508671
SNPdbe	rs397508671
MSV3d	rs397508671
GWAS Ctlg	rs397508671

Max Magnitude

0

ClinVar
Risk	rs397508671(-;-)
Alt	rs397508671(-;-)
Reference	Rs397508671(CTCC;CTCC)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117171088_117171091delCTCC
CLNSRC	ClinVar
CLNACC	RCV000047071.2,