rs387906833

Orientation

plus

Stabilized

plus

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

Make rs387906833(C;C)

Make rs387906833(C;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

27538049

Gene

RAB18

is a	snp
is	mentioned by
dbSNP	rs387906833
dbSNP (classic)	rs387906833
ClinGen	rs387906833
ebi	rs387906833
HLI	rs387906833
Exac	rs387906833
Gnomad	rs387906833
Varsome	rs387906833
LitVar	rs387906833
Map	rs387906833
PheGenI	rs387906833
Biobank	rs387906833
1000 genomes	rs387906833
hgdp	rs387906833
ensembl	rs387906833
geneview	rs387906833
scholar	rs387906833
google	rs387906833
pharmgkb	rs387906833
gwascentral	rs387906833
openSNP	rs387906833
23andMe	rs387906833
SNPshot	rs387906833
SNPdbe	rs387906833
MSV3d	rs387906833
GWAS Ctlg	rs387906833

Max Magnitude

0

ClinVar
Risk	rs387906833(A;A) rs387906833(C;C)
Alt	rs387906833(A;A) rs387906833(C;C)
Reference	Rs387906833(T;T)
Significance	Pathogenic
Disease	Warburg micro syndrome 3
Variation	info
Gene	RAB18
CLNDBN	Warburg micro syndrome 3
Reversed	0
HGVS	NC_000010.10:g.27826978T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023174.3,