rs267607234

Orientation

minus

Stabilized

minus

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

Make rs267607234(AA;AA)

Make rs267607234(AA;GG)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

64805745

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs267607234
dbSNP (classic)	rs267607234
ClinGen	rs267607234
ebi	rs267607234
HLI	rs267607234
Exac	rs267607234
Gnomad	rs267607234
Varsome	rs267607234
LitVar	rs267607234
Map	rs267607234
PheGenI	rs267607234
Biobank	rs267607234
1000 genomes	rs267607234
hgdp	rs267607234
ensembl	rs267607234
geneview	rs267607234
scholar	rs267607234
google	rs267607234
pharmgkb	rs267607234
gwascentral	rs267607234
openSNP	rs267607234
23andMe	rs267607234
SNPshot	rs267607234
SNPdbe	rs267607234
MSV3d	rs267607234
GWAS Ctlg	rs267607234

Max Magnitude

0

ClinVar
Risk	rs267607234(AA;AA)
Alt	rs267607234(AA;AA)
Reference	Rs267607234(GG;GG)
Significance	Pathogenic
Disease	Angiofibroma
Variation	info
Gene	MEN1
CLNDBN	Angiofibroma, somatic
Reversed	1
HGVS	NC_000011.9:g.64573217_64573218delCCinsTT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018175.4,