rs121908850

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs121908850(A;A)

Make rs121908850(A;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

34026832

Gene

ALG10

is a	snp
is	mentioned by
dbSNP	rs121908850
dbSNP (classic)	rs121908850
ClinGen	rs121908850
ebi	rs121908850
HLI	rs121908850
Exac	rs121908850
Gnomad	rs121908850
Varsome	rs121908850
LitVar	rs121908850
Map	rs121908850
PheGenI	rs121908850
Biobank	rs121908850
1000 genomes	rs121908850
hgdp	rs121908850
ensembl	rs121908850
geneview	rs121908850
scholar	rs121908850
google	rs121908850
pharmgkb	rs121908850
gwascentral	rs121908850
openSNP	rs121908850
23andMe	rs121908850
SNPshot	rs121908850
SNPdbe	rs121908850
MSV3d	rs121908850
GWAS Ctlg	rs121908850

Max Magnitude

0

OMIM	603313
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121908850(A;A)
Alt	rs121908850(A;A)
Reference	Rs121908850(G;G)
Significance	Other
Disease	Long QT syndrome 2
Variation	info
Gene	ALG10
CLNDBN	Long QT syndrome 2
Reversed	0
HGVS	NC_000012.11:g.34179767G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006869.2,