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rs781626187

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs781626187(A;C)
Make rs781626187(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position64016970
GeneLOC105369801, SRGAP1
is asnp
is mentioned by
dbSNPrs781626187
ebirs781626187
HLIrs781626187
Exacrs781626187
Varsomers781626187
Maprs781626187
PheGenIrs781626187
hapmaprs781626187
1000 genomesrs781626187
hgdprs781626187
ensemblrs781626187
gopubmedrs781626187
geneviewrs781626187
scholarrs781626187
googlers781626187
pharmgkbrs781626187
gwascentralrs781626187
openSNPrs781626187
23andMers781626187
23andMe allrs781626187
SNP Nexus

SNPshotrs781626187
SNPdbers781626187
MSV3drs781626187
GWAS Ctlgrs781626187
Max Magnitude0
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,