rs878853099

Orientation

minus

Stabilized

minus

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

Make rs878853099(A;G)

Make rs878853099(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

153869936

Gene

L1CAM

is a	snp
is	mentioned by
dbSNP	rs878853099
dbSNP (classic)	rs878853099
ClinGen	rs878853099
ebi	rs878853099
HLI	rs878853099
Exac	rs878853099
Gnomad	rs878853099
Varsome	rs878853099
LitVar	rs878853099
Map	rs878853099
PheGenI	rs878853099
Biobank	rs878853099
1000 genomes	rs878853099
hgdp	rs878853099
ensembl	rs878853099
geneview	rs878853099
scholar	rs878853099
google	rs878853099
pharmgkb	rs878853099
gwascentral	rs878853099
openSNP	rs878853099
23andMe	rs878853099
SNPshot	rs878853099
SNPdbe	rs878853099
MSV3d	rs878853099
GWAS Ctlg	rs878853099

Max Magnitude

0

ClinVar
Risk	rs878853099(G;G)
Alt	rs878853099(G;G)
Reference	Rs878853099(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	L1CAM
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153135391T>C
CLNSRC
CLNACC	RCV000224561.1,