rs104894257

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs104894257(A;A)

Make rs104894257(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

64807951

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs104894257
dbSNP (classic)	rs104894257
ClinGen	rs104894257
ebi	rs104894257
HLI	rs104894257
Exac	rs104894257
Gnomad	rs104894257
Varsome	rs104894257
LitVar	rs104894257
Map	rs104894257
PheGenI	rs104894257
Biobank	rs104894257
1000 genomes	rs104894257
hgdp	rs104894257
ensembl	rs104894257
geneview	rs104894257
scholar	rs104894257
google	rs104894257
pharmgkb	rs104894257
gwascentral	rs104894257
openSNP	rs104894257
23andMe	rs104894257
SNPshot	rs104894257
SNPdbe	rs104894257
MSV3d	rs104894257
GWAS Ctlg	rs104894257

Max Magnitude

0

OMIM	131100
Desc
Variant	0006
Related	also

ClinVar
Risk	rs104894257(A;A)
Alt	rs104894257(A;A)
Reference	Rs104894257(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MEN1
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.64575423C>T
CLNSRC
CLNACC	RCV000182450.1,