rs878855336

Orientation

minus

Stabilized

minus

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

Make rs878855336(A;A)

Make rs878855336(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

93133332

Gene

SAMD9L

is a	snp
is	mentioned by
dbSNP	rs878855336
dbSNP (classic)	rs878855336
ClinGen	rs878855336
ebi	rs878855336
HLI	rs878855336
Exac	rs878855336
Gnomad	rs878855336
Varsome	rs878855336
LitVar	rs878855336
Map	rs878855336
PheGenI	rs878855336
Biobank	rs878855336
1000 genomes	rs878855336
hgdp	rs878855336
ensembl	rs878855336
geneview	rs878855336
scholar	rs878855336
google	rs878855336
pharmgkb	rs878855336
gwascentral	rs878855336
openSNP	rs878855336
23andMe	rs878855336
SNPshot	rs878855336
SNPdbe	rs878855336
MSV3d	rs878855336
GWAS Ctlg	rs878855336

Max Magnitude

0

ClinVar
Risk	rs878855336(A;A) rs878855336(T;T)
Alt	rs878855336(A;A) rs878855336(T;T)
Reference	Rs878855336(C;C)
Significance	Pathogenic
Disease	Myelocerebellar disorder
Variation	info
Gene	SAMD9L
CLNDBN	Myelocerebellar disorder
Reversed	1
HGVS	NC_000007.13:g.92762645G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000234838.1,