rs397508618

Orientation

plus

Stabilized

plus

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

Make rs397508618(-;-)

Make rs397508618(-;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117642575

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508618
dbSNP (classic)	rs397508618
ClinGen	rs397508618
ebi	rs397508618
HLI	rs397508618
Exac	rs397508618
Gnomad	rs397508618
Varsome	rs397508618
LitVar	rs397508618
Map	rs397508618
PheGenI	rs397508618
Biobank	rs397508618
1000 genomes	rs397508618
hgdp	rs397508618
ensembl	rs397508618
geneview	rs397508618
scholar	rs397508618
google	rs397508618
pharmgkb	rs397508618
gwascentral	rs397508618
openSNP	rs397508618
23andMe	rs397508618
SNPshot	rs397508618
SNPdbe	rs397508618
MSV3d	rs397508618
GWAS Ctlg	rs397508618

Max Magnitude

0

ClinVar
Risk	rs397508618(-;-)
Alt	rs397508618(-;-)
Reference	Rs397508618(C;C)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117282629delC
CLNSRC	ClinVar
CLNACC	RCV000046998.2,