rs746460279

Merged into

rs121908786

Orientation

plus

Stabilized

plus

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

Make rs746460279(-;A)

Make rs746460279(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

117592212

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs746460279
dbSNP (classic)	rs746460279
ClinGen	rs746460279
ebi	rs746460279
HLI	rs746460279
Exac	rs746460279
Gnomad	rs746460279
Varsome	rs746460279
LitVar	rs746460279
Map	rs746460279
PheGenI	rs746460279
Biobank	rs746460279
1000 genomes	rs746460279
hgdp	rs746460279
ensembl	rs746460279
geneview	rs746460279
scholar	rs746460279
google	rs746460279
pharmgkb	rs746460279
gwascentral	rs746460279
openSNP	rs746460279
23andMe	rs746460279
SNPshot	rs746460279
SNPdbe	rs746460279
MSV3d	rs746460279
GWAS Ctlg	rs746460279

Status

Merged into rs121908786

Max Magnitude

0

ClinVar
Risk	rs746460279(A;A)
Alt	rs746460279(A;A)
Reference	Rs746460279(;)
Significance	Pathogenic
Disease	Cystic fibrosis not provided
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis not provided
Reversed	0
HGVS	NC_000007.13:g.117232273dupA
CLNSRC	CFTR2
CLNACC	RCV000029493.4, RCV000152995.3,