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rs786202100(CCTCA;CCTCA)

From SNPedia
common in clinvar
Is agenotype
ofrs786202100
GeneSDHB
Chromosome1
Position17,044,791
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;CCTCA) 6.2 Hereditary PGL/PCC Syndrome
(CCTCA;CCTCA) 0 common in clinvar
(I;I) 0 common genotype