rs397508806

Merged into

rs397508805

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AACTT;AACTT)	0	common in clinvar
(CTTAA;CTTAA)	0	common in clinvar

Make rs397508806(-;-)

Make rs397508806(-;CTTAA)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117536665

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508806
dbSNP (classic)	rs397508806
ClinGen	rs397508806
ebi	rs397508806
HLI	rs397508806
Exac	rs397508806
Gnomad	rs397508806
Varsome	rs397508806
LitVar	rs397508806
Map	rs397508806
PheGenI	rs397508806
Biobank	rs397508806
1000 genomes	rs397508806
hgdp	rs397508806
ensembl	rs397508806
geneview	rs397508806
scholar	rs397508806
google	rs397508806
pharmgkb	rs397508806
gwascentral	rs397508806
openSNP	rs397508806
23andMe	rs397508806
SNPshot	rs397508806
SNPdbe	rs397508806
MSV3d	rs397508806
GWAS Ctlg	rs397508806

Status

Merged into rs397508805

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs397508806(AACTT;AACTT)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117176719_117176723delCTTAA
CLNSRC	CFTR2
CLNACC	RCV000047272.5,