Original source

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


Chromosome 4: between 89809531 and 89809532 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs200957511

This variation has 24 HGVS names - click the plus to show

About this variant

This variant overlaps 22 transcripts and has 1 individual genotype.

Variation displays