Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]


Chromosome 18: between 44818993 and 44818994 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs202122294, rs61416824

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 3 individual genotypes.

Variation displays