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RET

From SNPedia
is agene
is mentioned by
EntrezGene5979
PheGenI5979
VariationViewer5979
ClinVarRET
GeneCardsRET
dbSNP5979
DiseasesRET
SADR5979
HugeNav5979
wikipediaRET
googleRET
gopubmedRET
EVSRET
HEFalMpRET
MyGene2RET
23andMeRET
# SNPs107
 Max MagnitudeChromosome positionSummary
rs1060500759043,120,162
rs121913308043,114,492
rs121913309043,120,165
rs121913312043,114,494
rs121913313043,113,630
rs142318626043,119,587
rs143795581043,114,596
rs143862573043,119,750
rs146646971043,114,598
rs17158558043,124,887
rs17857727043,100,520
rs1799939043,114,671
rs1800858043,100,520
rs1800860143,111,239
rs1800861043,118,395
rs1800862043,119,646
rs1800863043,120,185
rs186441043,080,177
rs193922699043,114,478
rs193922700043,114,680
rs201740483043,126,647
rs2075912043,126,769
rs2435357143,086,608
rs2472737043,120,057
rs250553543,097,595
rs250600443,086,825
rs250603042,952,399rs2506030 in RET is associated with higher risk in Hirschsprung disease (HSCR)
rs256520043,127,485
rs256520643,100,333
rs267607010043,114,497
rs267607011043,120,184
rs274223443,117,161
rs3026785043,130,238
rs34682185043,106,382
rs377767389043,112,120
rs377767391043,113,627
rs377767396043,113,623
rs377767397043,113,628
rs377767398043,113,628
rs377767400043,113,650
rs377767404043,114,488
rs377767405043,114,489
rs377767406043,114,491
rs377767408043,114,496
rs377767409043,114,501
rs377767416043,118,430
rs377767422043,119,635
rs377767426043,119,694
rs377767428043,120,120
rs377767429043,120,120
... further results


The RET gene has primarily been associated with risk for Hirschsprung disease.

SNPs in the RET gene associated with Hirschsprung disease include:

[PMID 21655256] Familial medullary thyroid carcinoma