Most severe consequence
22
synonymous variant
Alleles
C/G|MAF: 0 (N)|Highest population MAF: 0.03
Location
Chromosome 12:18785706 (forward strand)|VCF:12 18785706 tmp_12_18785706 C G
HGVS names
This variant has 3 HGVS names - Show
External Links
Original source
About this variant
This variant overlaps 1 transcript and has 20 sample genotypes.
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