rs781626187

Orientation

plus

Stabilized

plus

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

Make rs781626187(A;C)

Make rs781626187(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

64016970

Gene	LOC105369801, SRGAP1

is a	snp
is	mentioned by
dbSNP	rs781626187
dbSNP (classic)	rs781626187
ClinGen	rs781626187
ebi	rs781626187
HLI	rs781626187
Exac	rs781626187
Gnomad	rs781626187
Varsome	rs781626187
LitVar	rs781626187
Map	rs781626187
PheGenI	rs781626187
Biobank	rs781626187
1000 genomes	rs781626187
hgdp	rs781626187
ensembl	rs781626187
geneview	rs781626187
scholar	rs781626187
google	rs781626187
pharmgkb	rs781626187
gwascentral	rs781626187
openSNP	rs781626187
23andMe	rs781626187
SNPshot	rs781626187
SNPdbe	rs781626187
MSV3d	rs781626187
GWAS Ctlg	rs781626187

Max Magnitude

0

ClinVar
Risk	rs781626187(C;C)
Alt	rs781626187(C;C)
Reference	Rs781626187(A;A)
Significance	Pathogenic
Disease	Thyroid cancer
Variation	info
Gene	SRGAP1
CLNDBN	Thyroid cancer, follicular
Reversed	0
HGVS	NC_000012.11:g.64410750A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000190471.2,