Original source

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

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: 0.11 (A)
Location

Chromosome 19:41838206 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60826558

This variation has 12 HGVS names - click the plus to show

Variant allele A
19:g.41838206G>A
ENST00000221930.5:c.861-20C>T
ENST00000600196.1:n.173-20C>T
ENST00000598758.1:c.149-20C>T

Variant allele T
19:g.41838206G>T
ENST00000221930.5:c.861-20C>A
ENST00000600196.1:n.173-20C>A
ENST00000598758.1:c.149-20C>A

Variant allele C
19:g.41838206G>C
ENST00000221930.5:c.861-20C>G
ENST00000600196.1:n.173-20C>G
ENST00000598758.1:c.149-20C>G

This variation has assays on 7 chips - click the plus to show

Variation displays