rs1044812718

Orientation

plus

Stabilized

plus

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

Make rs1044812718(A;A)

Make rs1044812718(A;C)

Make rs1044812718(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

56453154

Gene

MIP

is a	snp
is	mentioned by
dbSNP	rs1044812718
dbSNP (classic)	rs1044812718
ClinGen	rs1044812718
ebi	rs1044812718
HLI	rs1044812718
Exac	rs1044812718
Gnomad	rs1044812718
Varsome	rs1044812718
LitVar	rs1044812718
Map	rs1044812718
PheGenI	rs1044812718
Biobank	rs1044812718
1000 genomes	rs1044812718
hgdp	rs1044812718
ensembl	rs1044812718
geneview	rs1044812718
scholar	rs1044812718
google	rs1044812718
pharmgkb	rs1044812718
gwascentral	rs1044812718
openSNP	rs1044812718
23andMe	rs1044812718
SNPshot	rs1044812718
SNPdbe	rs1044812718
MSV3d	rs1044812718
GWAS Ctlg	rs1044812718

Max Magnitude

0

ClinVar
Risk	rs1044812718(A;A)
Alt	rs1044812718(A;A)
Reference	Rs1044812718(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MIP
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.56846938T>G
CLNSRC
CLNACC	RCV000430035.1,