rs104894171

Orientation

plus

Stabilized

plus

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

Make rs104894171(A;G)

Make rs104894171(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

87508507

Gene

MINPP1

is a	snp
is	mentioned by
dbSNP	rs104894171
dbSNP (classic)	rs104894171
ClinGen	rs104894171
ebi	rs104894171
HLI	rs104894171
Exac	rs104894171
Gnomad	rs104894171
Varsome	rs104894171
LitVar	rs104894171
Map	rs104894171
PheGenI	rs104894171
Biobank	rs104894171
1000 genomes	rs104894171
hgdp	rs104894171
ensembl	rs104894171
geneview	rs104894171
scholar	rs104894171
google	rs104894171
pharmgkb	rs104894171
gwascentral	rs104894171
openSNP	rs104894171
23andMe	rs104894171
SNPshot	rs104894171
SNPdbe	rs104894171
MSV3d	rs104894171
GWAS Ctlg	rs104894171

Max Magnitude

0

OMIM	605391
Desc
Variant	0002
Related	also

ClinVar
Risk	rs104894171(G;G)
Alt	rs104894171(G;G)
Reference	Rs104894171(A;A)
Significance	Pathogenic
Disease	Thyroid cancer
Variation	info
Gene	MINPP1
CLNDBN	Thyroid cancer, follicular
Reversed	0
HGVS	NC_000010.10:g.89268264A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005325.2,