rs761695866

Orientation

plus

Stabilized

plus

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

Make rs761695866(-;C)

Make rs761695866(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

64804618

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs761695866
dbSNP (classic)	rs761695866
ClinGen	rs761695866
ebi	rs761695866
HLI	rs761695866
Exac	rs761695866
Gnomad	rs761695866
Varsome	rs761695866
LitVar	rs761695866
Map	rs761695866
PheGenI	rs761695866
Biobank	rs761695866
1000 genomes	rs761695866
hgdp	rs761695866
ensembl	rs761695866
geneview	rs761695866
scholar	rs761695866
google	rs761695866
pharmgkb	rs761695866
gwascentral	rs761695866
openSNP	rs761695866
23andMe	rs761695866
SNPshot	rs761695866
SNPdbe	rs761695866
MSV3d	rs761695866
GWAS Ctlg	rs761695866

Max Magnitude

0

ClinVar
Risk	rs761695866(C;C)
Alt	rs761695866(C;C)
Reference	Rs761695866(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MAP4K2 MEN1
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.64572091dupC
CLNSRC
CLNACC	RCV000182442.1,