Original source

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


Chromosome 7: between 103858002 and 103858003 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs200006453, rs142568772

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 5 individual genotypes.

Variation displays