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rs797044990

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044990(A;A)
Make rs797044990(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position64062938
GeneSRGAP1
is asnp
is mentioned by
dbSNPrs797044990
ebirs797044990
HLIrs797044990
Exacrs797044990
Varsomers797044990
Maprs797044990
PheGenIrs797044990
hapmaprs797044990
1000 genomesrs797044990
hgdprs797044990
ensemblrs797044990
gopubmedrs797044990
geneviewrs797044990
scholarrs797044990
googlers797044990
pharmgkbrs797044990
gwascentralrs797044990
openSNPrs797044990
23andMers797044990
23andMe allrs797044990
SNP Nexus

SNPshotrs797044990
SNPdbers797044990
MSV3drs797044990
GWAS Ctlgrs797044990
Max Magnitude0
ClinVar
Risk rs797044990(A;A)
Alt rs797044990(A;A)
Reference rs797044990(G;G)
Significance Pathogenic
Disease Thyroid cancer
Variation info
Gene SRGAP1
CLNDBN Thyroid cancer, follicular
Reversed 0
HGVS NC_000012.11:g.64456718G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190472.2,