Original source

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


Chromosome 14: between 100839948 and 100839949 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs67674945, rs141031319

This variation has 44 HGVS names - click the plus to show

About this variant

This variant overlaps 46 transcripts and has 1 individual genotype.

Variation displays