Original source

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

Alleles
T/C | Ambiguity code: Y
Location

Chromosome 4:136443949 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

Variation displays