rs538912281

Orientation

plus

Stabilized

plus

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

Make rs538912281(C;G)

Make rs538912281(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

97854657

Gene

FOXE1

is a	snp
is	mentioned by
dbSNP	rs538912281
dbSNP (classic)	rs538912281
ClinGen	rs538912281
ebi	rs538912281
HLI	rs538912281
Exac	rs538912281
Gnomad	rs538912281
Varsome	rs538912281
LitVar	rs538912281
Map	rs538912281
PheGenI	rs538912281
Biobank	rs538912281
1000 genomes	rs538912281
hgdp	rs538912281
ensembl	rs538912281
geneview	rs538912281
scholar	rs538912281
google	rs538912281
pharmgkb	rs538912281
gwascentral	rs538912281
openSNP	rs538912281
23andMe	rs538912281
SNPshot	rs538912281
SNPdbe	rs538912281
MSV3d	rs538912281
GWAS Ctlg	rs538912281

Max Magnitude

0

ClinVar
Risk	rs538912281(G;G)
Alt	rs538912281(G;G)
Reference	Rs538912281(C;C)
Significance	Pathogenic
Disease	Thyroid cancer
Variation	info
Gene	FOXE1 LOC101928337
CLNDBN	Thyroid cancer, nonmedullary, 4
Reversed	0
HGVS	NC_000009.11:g.100616939C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000190467.2,