Original source

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


Chromosome 1: between 26756564 and 26756565 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs66846392, rs66846391

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

About this variant

This variant overlaps 4 transcripts and has 1 individual genotype.

Variation displays