rs786204625

Orientation

plus

Stabilized

plus

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

Make rs786204625(-;-)

Make rs786204625(-;A)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

19663492

Gene

ALDH3A2

is a	snp
is	mentioned by
dbSNP	rs786204625
dbSNP (classic)	rs786204625
ClinGen	rs786204625
ebi	rs786204625
HLI	rs786204625
Exac	rs786204625
Gnomad	rs786204625
Varsome	rs786204625
LitVar	rs786204625
Map	rs786204625
PheGenI	rs786204625
Biobank	rs786204625
1000 genomes	rs786204625
hgdp	rs786204625
ensembl	rs786204625
geneview	rs786204625
scholar	rs786204625
google	rs786204625
pharmgkb	rs786204625
gwascentral	rs786204625
openSNP	rs786204625
23andMe	rs786204625
SNPshot	rs786204625
SNPdbe	rs786204625
MSV3d	rs786204625
GWAS Ctlg	rs786204625

Max Magnitude

0

ClinVar
Risk	rs786204625(-;-)
Alt	rs786204625(-;-)
Reference	Rs786204625(A;A)
Significance	Probable-Pathogenic
Disease	Sjögren-Larsson syndrome
Variation	info
Gene	ALDH3A2
CLNDBN	Sjögren-Larsson syndrome
Reversed	0
HGVS	NC_000017.10:g.19566805delA
CLNSRC
CLNACC	RCV000169395.1,