Most severe consequence
28
intron variant
Alleles
A/G
Location
Chromosome 1:4496678 (forward strand)|VCF:1 4496678 rs53023920 A G
HGVS names
This variant has 2 HGVS names - Show
External Links
Original source
About this variant
This variant overlaps 1 transcript and has 1 sample genotype.
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