rs786205618

Orientation

minus

Stabilized

minus

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

Make rs786205618(-;-)

Make rs786205618(-;CTT)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

124923384

Gene	HEPACAM, LOC107984406

is a	snp
is	mentioned by
dbSNP	rs786205618
dbSNP (classic)	rs786205618
ClinGen	rs786205618
ebi	rs786205618
HLI	rs786205618
Exac	rs786205618
Gnomad	rs786205618
Varsome	rs786205618
LitVar	rs786205618
Map	rs786205618
PheGenI	rs786205618
Biobank	rs786205618
1000 genomes	rs786205618
hgdp	rs786205618
ensembl	rs786205618
geneview	rs786205618
scholar	rs786205618
google	rs786205618
pharmgkb	rs786205618
gwascentral	rs786205618
openSNP	rs786205618
23andMe	rs786205618
SNPshot	rs786205618
SNPdbe	rs786205618
MSV3d	rs786205618
GWAS Ctlg	rs786205618

Max Magnitude

0

ClinVar
Risk	rs786205618(-;-)
Alt	rs786205618(-;-)
Reference	Rs786205618(CTT;CTT)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HEPACAM
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.124793280_124793282delAAG
CLNSRC
CLNACC	RCV000171466.1,