Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
-/G/T
Location

Chromosome 5: between 147475513 and 147475514 (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

Variation displays