Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: < 0.01 (T)
Location

Chromosome 4:147558090 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.147558090G>T

Variation displays