Original source

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


Chromosome 14: between 92096910 and 92096911 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs71123315

This variation has 50 HGVS names - click the plus to show

About this variant

This variant overlaps 51 transcripts and has 3 individual genotypes.

Variation displays