Original source

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


Chromosome 8: between 23058491 and 23058492 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs370466030, rs200849711

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 7 individual genotypes.

Variation displays