rs397508366

Merged into

rs397508360

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(;)	0	common in clinvar
(-;-)	0	common/normal
(-;T)	3	carrier of a cystic fibrosis allele

Make rs397508366(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117509102

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508366
dbSNP (classic)	rs397508366
ClinGen	rs397508366
ebi	rs397508366
HLI	rs397508366
Exac	rs397508366
Gnomad	rs397508366
Varsome	rs397508366
LitVar	rs397508366
Map	rs397508366
PheGenI	rs397508366
Biobank	rs397508366
1000 genomes	rs397508366
hgdp	rs397508366
ensembl	rs397508366
geneview	rs397508366
scholar	rs397508366
google	rs397508366
pharmgkb	rs397508366
gwascentral	rs397508366
openSNP	rs397508366
23andMe	rs397508366
SNPshot	rs397508366
SNPdbe	rs397508366
MSV3d	rs397508366
GWAS Ctlg	rs397508366

Status

Merged into rs397508360

Max Magnitude

3

ClinVar
Risk	rs397508366(T;T)
Alt	rs397508366(T;T)
Reference	Rs397508366(;)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117149156dupT
CLNSRC	CFTR2
CLNACC	RCV000046577.6,