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rs672601328

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs672601328(-;-)
Make rs672601328(-;AGGAGTGTG)
Make rs672601328(AGGAGTGTG;AGGAGTGTG)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position43112170
GeneRET
is asnp
is mentioned by
dbSNPrs672601328
ebirs672601328
HLIrs672601328
Exacrs672601328
Varsomers672601328
Maprs672601328
PheGenIrs672601328
hapmaprs672601328
1000 genomesrs672601328
hgdprs672601328
ensemblrs672601328
gopubmedrs672601328
geneviewrs672601328
scholarrs672601328
googlers672601328
pharmgkbrs672601328
gwascentralrs672601328
openSNPrs672601328
23andMers672601328
23andMe allrs672601328
SNP Nexus

SNPshotrs672601328
SNPdbers672601328
MSV3drs672601328
GWAS Ctlgrs672601328
Max Magnitude0
ClinVar
Risk rs672601328(GGAGTGTGA;GGAGTGTGA)
Alt rs672601328(GGAGTGTGA;GGAGTGTGA)
Reference rs672601328(;)
Significance Pathogenic
Disease Familial medullary thyroid carcinoma
Variation info
Gene RET
CLNDBN Familial medullary thyroid carcinoma
Reversed 0
HGVS NC_000010.10:g.43607610_43607618dupAGGAGTGTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000014968.26,