rs794728660

Orientation

minus

Stabilized

minus

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

Make rs794728660(-;GGCTCAGGTGCCAGCAC)

Make rs794728660(GGCTCAGGTGCCAGCAC;GGCTCAGGTGCCAGCAC)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

64804548

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs794728660
dbSNP (classic)	rs794728660
ClinGen	rs794728660
ebi	rs794728660
HLI	rs794728660
Exac	rs794728660
Gnomad	rs794728660
Varsome	rs794728660
LitVar	rs794728660
Map	rs794728660
PheGenI	rs794728660
Biobank	rs794728660
1000 genomes	rs794728660
hgdp	rs794728660
ensembl	rs794728660
geneview	rs794728660
scholar	rs794728660
google	rs794728660
pharmgkb	rs794728660
gwascentral	rs794728660
openSNP	rs794728660
23andMe	rs794728660
SNPshot	rs794728660
SNPdbe	rs794728660
MSV3d	rs794728660
GWAS Ctlg	rs794728660

Max Magnitude

0

ClinVar
Risk	rs794728660(GGCTCAGGTGCCAGCAC;GGCTCAGGTGCCAGCAC)
Alt	rs794728660(GGCTCAGGTGCCAGCAC;GGCTCAGGTGCCAGCAC)
Reference	Rs794728660(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MAP4K2 MEN1
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.64572021_64572037dup17
CLNSRC
CLNACC	RCV000182463.1,