rs61759860

Orientation

minus

Stabilized

minus

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

Make rs61759860(C;T)

Make rs61759860(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

6374543

Gene	LOC105369626, LTBR, SCNN1A

is a	snp
is	mentioned by
dbSNP	rs61759860
dbSNP (classic)	rs61759860
ClinGen	rs61759860
ebi	rs61759860
HLI	rs61759860
Exac	rs61759860
Gnomad	rs61759860
Varsome	rs61759860
LitVar	rs61759860
Map	rs61759860
PheGenI	rs61759860
Biobank	rs61759860
1000 genomes	rs61759860
hgdp	rs61759860
ensembl	rs61759860
geneview	rs61759860
scholar	rs61759860
google	rs61759860
pharmgkb	rs61759860
gwascentral	rs61759860
openSNP	rs61759860
23andMe	rs61759860
SNPshot	rs61759860
SNPdbe	rs61759860
MSV3d	rs61759860
GWAS Ctlg	rs61759860

Max Magnitude

0

OMIM	600228
Desc
Variant	0008
Related	also

ClinVar
Risk	rs61759860(T;T)
Alt	rs61759860(T;T)
Reference	Rs61759860(C;C)
Significance	Pathogenic
Disease	Bronchiectasis with or without elevated sweat chloride 2
Variation	info
Gene	SCNN1A LTBR
CLNDBN	Bronchiectasis with or without elevated sweat chloride 2
Reversed	1
HGVS	NC_000012.11:g.6483709G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009852.5,