rs397508206

Orientation

plus

Stabilized

plus

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

Make rs397508206(-;-)

Make rs397508206(-;CA)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117559504

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508206
dbSNP (classic)	rs397508206
ClinGen	rs397508206
ebi	rs397508206
HLI	rs397508206
Exac	rs397508206
Gnomad	rs397508206
Varsome	rs397508206
LitVar	rs397508206
Map	rs397508206
PheGenI	rs397508206
Biobank	rs397508206
1000 genomes	rs397508206
hgdp	rs397508206
ensembl	rs397508206
geneview	rs397508206
scholar	rs397508206
google	rs397508206
pharmgkb	rs397508206
gwascentral	rs397508206
openSNP	rs397508206
23andMe	rs397508206
SNPshot	rs397508206
SNPdbe	rs397508206
MSV3d	rs397508206
GWAS Ctlg	rs397508206

Max Magnitude

0

ClinVar
Risk	rs397508206(-;-)
Alt	rs397508206(-;-)
Reference	Rs397508206(CA;CA)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117199558_117199559delCA
CLNSRC	ClinVar
CLNACC	RCV000046301.2,