Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/G/T
Location

Chromosome 5: between 148095950 and 148095951 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs142972606

This variation has 20 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts and has 2 individual genotypes.

Variation displays