rs786205614

Orientation

minus

Stabilized

minus

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

Make rs786205614(A;G)

Make rs786205614(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

95637408

Gene

ALDH18A1

is a	snp
is	mentioned by
dbSNP	rs786205614
dbSNP (classic)	rs786205614
ClinGen	rs786205614
ebi	rs786205614
HLI	rs786205614
Exac	rs786205614
Gnomad	rs786205614
Varsome	rs786205614
LitVar	rs786205614
Map	rs786205614
PheGenI	rs786205614
Biobank	rs786205614
1000 genomes	rs786205614
hgdp	rs786205614
ensembl	rs786205614
geneview	rs786205614
scholar	rs786205614
google	rs786205614
pharmgkb	rs786205614
gwascentral	rs786205614
openSNP	rs786205614
23andMe	rs786205614
SNPshot	rs786205614
SNPdbe	rs786205614
MSV3d	rs786205614
GWAS Ctlg	rs786205614

Max Magnitude

0

ClinVar
Risk	rs786205614(G;G)
Alt	rs786205614(G;G)
Reference	Rs786205614(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ALDH18A1
CLNDBN	not provided
Reversed	1
HGVS	NC_000010.10:g.97397165T>C
CLNSRC
CLNACC	RCV000171459.1,