Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.45 (T)
Location

Chromosome 4:88078154 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17731031, rs57055011

HGVS name

4:g.88078154T>G

This variation has assays on 9 chips - click the plus to show

Variation displays