Original source

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


Chromosome 1: between 236815695 and 236815696 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs200394864, rs112130300

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 10 individual genotypes.

Variation displays