Original source

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

Alleles
-/G/T
Location

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

Co-located
Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs142972606

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

Variation displays